BIOCHEMIC TISSUE SALT KIT
cell salts kit |
| Product Information |
| Product Type | HUMAN OTC DRUG | Item Code (Source) | NDC: 85816-1201 |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1201-1 | 1 in 1 KIT; Type 1: Convenience Kit of Co-Package | 01/01/2015 | |
|
| Quantity of Parts |
| Part # | Package Quantity | Total Product Quantity |
| Part 1 | 1 BOTTLE, GLASS | 30000 mg |
| Part 2 | 1 BOTTLE, GLASS | 30000 mg |
| Part 3 | 1 BOTTLE, GLASS | 30000 mg |
| Part 4 | 1 BOTTLE, GLASS | 30000 mg |
| Part 5 | 1 BOTTLE, GLASS | 30000 mg |
| Part 6 | 1 BOTTLE, GLASS | 30000 mg |
| Part 7 | 1 BOTTLE, GLASS | 30000 mg |
| Part 8 | 1 BOTTLE, GLASS | 30000 mg |
| Part 9 | 1 BOTTLE, GLASS | 30000 mg |
| Part 10 | 1 BOTTLE, GLASS | 30000 mg |
| Part 11 | 1 BOTTLE, GLASS | 30000 mg |
| Part 12 | 1 BOTTLE, GLASS | 30000 mg |
|
| Part 1 of 12 |
BM KALI SULPH
kali sulphuricum tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1007 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| POTASSIUM SULFATE (UNII: 1K573LC5TV) (POTASSIUM CATION - UNII:295O53K152) | POTASSIUM SULFATE | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1007-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 2 of 12 |
BM MAG PHOS
magnesium phosphate tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1008 |
| 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 | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1008-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 3 of 12 |
BM FERR PHOS
ferrum phosphoricum tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1004 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) | FERROSOFERRIC PHOSPHATE | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1004-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 4 of 12 |
BM NAT MUR
natrium muriaticum tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1009 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) | SODIUM CHLORIDE | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1009-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 5 of 12 |
BM NAT PHOS
natrum phosphoricum tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1010 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B) (PHOSPHATE ION - UNII:NK08V8K8HR) | SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1010-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 6 of 12 |
BM CALC FLUOR
calcarea fluorica tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1001 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) | CALCIUM FLUORIDE | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1001-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 7 of 12 |
BM CALC PHOS
calcarea phosphorica tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1002 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (PHOSPHATE ION - UNII:NK08V8K8HR) | TRIBASIC CALCIUM PHOSPHATE | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1002-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 8 of 12 |
BM KALI MUR
kali muriaticum tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1005 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) | POTASSIUM CHLORIDE | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1005-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 9 of 12 |
BM KALI PHOS
kali phosphoricum tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1006 |
| 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 | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1006-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 10 of 12 |
BM NAT SULPH
natrum sulphuricum tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1011 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM CATION - UNII:LYR4M0NH37) | SODIUM SULFATE | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1011-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 11 of 12 |
BM SILICEA
silicea tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1012 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) | SILICON DIOXIDE | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1012-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
| Part 12 of 12 |
BM CALC SULPH
calcarea sulphurica tablet |
|
| Product Information |
| Item Code (Source) | NDC: 85816-1003 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB) | CALCIUM SULFATE ANHYDROUS | 6 [hp_X] in 60 mg |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MAGNESIUM STEARATE (UNII: 70097M6I30) | 1.25 mg in 60 mg |
| LACTOSE (UNII: J2B2A4N98G) | 58.6 mg in 60 mg |
|
| Product Characteristics |
| Color | white | Score | no score |
| Shape | ROUND | Size | 90mm |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 85816-1003-1 | 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved homeopathic | | 01/01/2015 | |
|