200C HOMEOPATHIC REMEDY KIT
50 remedy kit kit |
| Product Information |
| Product Type | HUMAN OTC DRUG | Item Code (Source) | NDC: 71919-822 |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-822-18 | 50 in 1 KIT | 02/29/2024 | |
| 1 | NDC: 71919-822-01 | 1 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
| Quantity of Parts |
| Part # | Package Quantity | Total Product Quantity |
| Part 1 | 1 VIAL, GLASS | 750 |
| Part 2 | 1 VIAL, GLASS | 350 |
| Part 3 | 1 VIAL, GLASS | 750 |
| Part 4 | 1 VIAL, GLASS | 750 |
| Part 5 | 1 VIAL, GLASS | 750 |
| Part 6 | 1 VIAL, GLASS | 750 |
| Part 7 | 1 VIAL, GLASS | 750 |
| Part 8 | 1 VIAL, GLASS | 750 |
| Part 9 | 1 VIAL, GLASS | 350 |
| Part 10 | 1 VIAL, GLASS | 350 |
| Part 11 | 1 VIAL, GLASS | 750 |
| Part 12 | 1 VIAL, GLASS | 750 |
| Part 13 | 1 VIAL, GLASS | 750 |
| Part 14 | 1 VIAL, GLASS | 750 |
| Part 15 | 1 VIAL, GLASS | 750 |
| Part 16 | 1 VIAL, GLASS | 350 |
| Part 17 | 1 VIAL, GLASS | 750 |
| Part 18 | 1 VIAL, GLASS | 350 |
| Part 19 | 1 VIAL, GLASS | 350 |
| Part 20 | 1 VIAL, GLASS | 750 |
| Part 21 | 1 VIAL, GLASS | 750 |
| Part 22 | 1 VIAL, GLASS | 750 |
| Part 23 | 1 VIAL, GLASS | 350 |
| Part 24 | 1 VIAL, GLASS | 750 |
| Part 25 | 1 VIAL, GLASS | 350 |
| Part 26 | 1 VIAL, GLASS | 750 |
| Part 27 | 1 VIAL, GLASS | 750 |
| Part 28 | 1 VIAL, GLASS | 750 |
| Part 29 | 1 VIAL, GLASS | 750 |
| Part 30 | 1 VIAL, GLASS | 350 |
| Part 31 | 1 VIAL, GLASS | 750 |
| Part 32 | 1 VIAL, GLASS | 350 |
| Part 33 | 1 VIAL, GLASS | 750 |
| Part 34 | 1 VIAL, GLASS | 750 |
| Part 35 | 1 VIAL, GLASS | 750 |
| Part 36 | 1 VIAL, GLASS | 750 |
| Part 37 | 1 VIAL, GLASS | 750 |
| Part 38 | 1 VIAL, GLASS | 750 |
| Part 39 | 1 VIAL, GLASS | 350 |
| Part 40 | 1 VIAL, GLASS | 750 |
| Part 41 | 1 VIAL, GLASS | 750 |
| Part 42 | 1 VIAL, GLASS | 350 |
| Part 43 | 1 VIAL, GLASS | 750 |
| Part 44 | 1 VIAL, GLASS | 750 |
| Part 45 | 1 VIAL, GLASS | 750 |
| Part 46 | 1 VIAL, GLASS | 750 |
| Part 47 | 1 VIAL, GLASS | 750 |
| Part 48 | 1 VIAL, GLASS | 750 |
| Part 49 | 1 VIAL, GLASS | 750 |
| Part 50 | 1 VIAL, GLASS | 750 |
|
| Part 1 of 50 |
ACONITUM NAPELLUS KIT REFILL
aconitum napellus pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-026 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) | ACONITUM NAPELLUS | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-026-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 2 of 50 |
AESCULUS HIPP KIT REFILL
horse chestnut pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-759 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| HORSE CHESTNUT (UNII: 3C18L6RJAZ) (HORSE CHESTNUT - UNII:3C18L6RJAZ) | HORSE CHESTNUT | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-759-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 05/05/2022 | |
|
| Part 3 of 50 |
ALLIUM CEPA KIT REFILL
onion pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-028 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) | ONION | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-028-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 4 of 50 |
ANTIMONIUM CRUDUM KIT REFILL
antimony trisulfide pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-812 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) | ANTIMONY TRISULFIDE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-812-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 11/07/2023 | |
|
| Part 5 of 50 |
APIS MELLIFICA KIT REFILL
apis mellifera pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-030 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) | APIS MELLIFERA | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-030-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 6 of 50 |
ARNICA MONTANA KIT REFILL
arnica montana pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-032 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) | ARNICA MONTANA | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-032-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 7 of 50 |
ARSENICUM ALBUM KIT REFILL
arsenic trioxide pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-033 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) | ARSENIC TRIOXIDE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-033-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 8 of 50 |
BELLADONNA KIT REFILL
atropa belladonna pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-034 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) | ATROPA BELLADONNA | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-034-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 9 of 50 |
BELLIS PERENNIS KIT REFILL
bellis perennis pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-773 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| BELLIS PERENNIS (UNII: 2HU33I03UY) (BELLIS PERENNIS - UNII:2HU33I03UY) | BELLIS PERENNIS | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-773-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 06/10/2022 | |
|
| Part 10 of 50 |
BERBERIS VULGARIS KIT REFILL
berberis vulgaris root bark pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-762 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) | BERBERIS VULGARIS ROOT BARK | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-762-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 05/10/2022 | |
|
| Part 11 of 50 |
BRYONIA ALBA KIT REFILL
bryonia alba root pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-035 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) | BRYONIA ALBA ROOT | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-035-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 12 of 50 |
CALCAREA CARBONICA KIT REFILL
oyster shell calcium carbonate, crude pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-036 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) | OYSTER SHELL CALCIUM CARBONATE, CRUDE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-036-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 13 of 50 |
CAULOPHYLLUM THAL KIT REFILL
caulophyllum thalictroides root pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-040 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH) (CAULOPHYLLUM THALICTROIDES ROOT - UNII:JTJ6HH6YEH) | CAULOPHYLLUM THALICTROIDES ROOT | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-040-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 14 of 50 |
CAUSTICUM KIT REFILL
causticum pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-041 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU) | CAUSTICUM | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-041-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 15 of 50 |
CHAMOMILLA KIT REFILL
matricaria recutita pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-042 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) | MATRICARIA RECUTITA | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-042-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 16 of 50 |
CIMICIFUGA RACEMOSA KIT REFILL
black cohosh pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-767 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9) | BLACK COHOSH | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-767-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 05/25/2022 | |
|
| Part 17 of 50 |
COFFEA CRUDA KIT REFILL
arabica coffee bean pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-045 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| ARABICA COFFEE BEAN (UNII: 3SW678MX72) (ARABICA COFFEE BEAN - UNII:3SW678MX72) | ARABICA COFFEE BEAN | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-045-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 10/06/2010 | |
|
| Part 18 of 50 |
DROSERA ROTUNDIFOLIA KIT REFILL
drosera rotundifolia pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-761 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (DROSERA ROTUNDIFOLIA FLOWERING TOP - UNII:75O014T1HG) | DROSERA ROTUNDIFOLIA FLOWERING TOP | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-761-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 05/10/2022 | |
|
| Part 19 of 50 |
EUPATORIUM PERF KIT REFILL
eupatorium perfoliatum flowering top pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-766 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E) | EUPATORIUM PERFOLIATUM FLOWERING TOP | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-766-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 05/25/2022 | |
|
| Part 20 of 50 |
EUPHRASIA OFFICINALIS KIT REFILL
euphrasia stricta pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-047 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) | EUPHRASIA STRICTA | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-047-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 21 of 50 |
FERRUM PHOS KIT REFILL
ferrum phosphoricum pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-048 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) | FERROSOFERRIC PHOSPHATE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-048-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 22 of 50 |
GELSEMIUM SEMP KIT REFILL
gelsemium sempervirens root pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-049 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) | GELSEMIUM SEMPERVIRENS ROOT | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-049-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 23 of 50 |
HAMAMELIS VIRGINIANA KIT REFILL
hamamelis virginiana root bark/stem bark pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-760 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) | HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-760-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 05/10/2022 | |
|
| Part 24 of 50 |
HEPAR SULPH CALC KIT REFILL
calcium sulfide pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-051 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) | CALCIUM SULFIDE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-051-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 25 of 50 |
HYDRASTIS CANADENSIS
goldenseal pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-763 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) | GOLDENSEAL | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-763-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 05/25/2022 | |
|
| Part 26 of 50 |
HYPERICUM PERF KIT REFILL
hypericum perforatum pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-052 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) | HYPERICUM PERFORATUM | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-052-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 27 of 50 |
IGNATIA AMARA KIT REFILL
strychnos ignatii seed pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-053 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (STRYCHNOS IGNATII SEED - UNII:1NM3M2487K) | STRYCHNOS IGNATII SEED | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-053-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 28 of 50 |
IPECACUANHA KIT REFILL
ipecac pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-054 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) | IPECAC | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-054-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 29 of 50 |
KALI BICHROMICUM KIT REFILL
potassium dichromate pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-055 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) | POTASSIUM DICHROMATE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-055-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 30 of 50 |
KALI CARBONICUM KIT REFILL
potassium carbonate pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-769 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) | POTASSIUM CARBONATE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-769-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 05/25/2022 | |
|
| Part 31 of 50 |
KALI MURIATICUM KIT REFILL
potassium chloride pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-813 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) | POTASSIUM CHLORIDE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-813-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 11/07/2023 | |
|
| Part 32 of 50 |
KALI PHOSPHORICUM KIT REFILL
potassium phosphate, dibasic pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-777 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR) | POTASSIUM PHOSPHATE, DIBASIC | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-777-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 09/23/2022 | |
|
| Part 33 of 50 |
LACHESIS MUTUS KIT REFILL
lachesis muta venom pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-056 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) | LACHESIS MUTA VENOM | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-056-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 34 of 50 |
LEDUM PALUSTRE KIT REFILL
ledum palustre twig pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-057 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P) | LEDUM PALUSTRE TWIG | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-057-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 35 of 50 |
LYCOPODIUM KIT REFILL
lycopodium clavatum spore pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-058 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) | LYCOPODIUM CLAVATUM SPORE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-058-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 36 of 50 |
MAGNESIA PHOS KIT REFILL
magnesium phosphate, dibasic trihydrate pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-059 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) | MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-059-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 37 of 50 |
NATRUM MURIATICUM KIT REFILL
sodium chloride pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-061 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) | SODIUM CHLORIDE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-061-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 38 of 50 |
NUX VOMICA KIT REFILL
strychnos nux-vomica seed pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-062 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) | STRYCHNOS NUX-VOMICA SEED | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-062-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 39 of 50 |
PETROLEUM KIT REFILL
kerosene pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-770 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) | KEROSENE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-770-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 05/25/2022 | |
|
| Part 40 of 50 |
PHOSPHORICUM ACIDUM KIT REFILL
phosphoric acid pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-814 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) | PHOSPHORIC ACID | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-814-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 11/07/2023 | |
|
| Part 41 of 50 |
PHYTOLACCA KIT REFILL
phytolacca americana root pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-064 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG) | PHYTOLACCA AMERICANA ROOT | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-064-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 42 of 50 |
PODOPHYLLUM PELT KIT REFILL
podophyllum pellet |
|
| Product Information |
| Item Code (Source) | NDC: 71919-771 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| PODOPHYLLUM PELTATUM ROOT (UNII: 2S713A4VP3) (PODOPHYLLUM PELTATUM ROOT - UNII:2S713A4VP3) | PODOPHYLLUM PELTATUM ROOT | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 71919-771-01 | 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 05/25/2022 | |
|
| Part 43 of 50 |
PULSATILLA KIT REFILL
pulsatilla vulgaris pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-065 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) | PULSATILLA VULGARIS | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-065-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 44 of 50 |
RHUS TOX KIT REFILL
toxicodendron radicans leaf pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-067 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| TOXICODENDRON RADICANS LEAF (UNII: CDH3461U7L) (TOXICODENDRON RADICANS LEAF - UNII:CDH3461U7L) | TOXICODENDRON RADICANS LEAF | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-067-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 45 of 50 |
RUTA GRAVEOLENS KIT REFILL
ruta graveolens flowering top pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-068 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) | RUTA GRAVEOLENS FLOWERING TOP | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-068-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 46 of 50 |
SEPIA KIT REFILL
sepia officinalis juice pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-069 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) | SEPIA OFFICINALIS JUICE | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-069-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 47 of 50 |
STAPHYSAGRIA KIT REFILL
delphinium staphisagria seed pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-072 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (DELPHINIUM STAPHISAGRIA SEED - UNII:00543AP1JV) | DELPHINIUM STAPHISAGRIA SEED | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-072-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 48 of 50 |
SULPHUR KIT REFILL
sulfur pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-073 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) | SULFUR | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-073-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 49 of 50 |
SYMPHYTUM OFF KIT REFILL
comfrey root pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-074 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) | COMFREY ROOT | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| SUCROSE (UNII: C151H8M554) | |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-074-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
| Part 50 of 50 |
THUJA OCCIDENTALIS KIT REFILL
thuja occidentalis leafy twig pellet |
|
| Product Information |
| Item Code (Source) | NDC: 68428-075 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) | THUJA OCCIDENTALIS LEAFY TWIG | 200 [hp_C] |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) | |
| SUCROSE (UNII: C151H8M554) | |
|
| Product Characteristics |
| Color | white (white) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 68428-075-01 | 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 12/06/2010 | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 02/29/2024 | |
|