MODEL 6240-35-001CS
first aid kit with drug kit |
| Product Information |
| Product Type | MEDICAL DEVICE | Item Code (Source) | NHRIC:27860-012 |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NHRIC:27860-012-09 | 1 in 1 PACKAGE; Type 1: Convenience Kit of Co-Package | | |
|
| Quantity of Parts |
| Part # | Package Quantity | Total Product Quantity |
| Part 1 | | 1 |
| Part 2 | | 1 |
| Part 3 | | 1 |
| Part 4 | | 1 |
| Part 5 | | 1 |
| Part 6 | | 1 |
| Part 7 | | 1 |
| Part 8 | | 1 |
| Part 9 | | 1 |
|
| Part 1 of 9 |
MOORE MEDICAL NON ASPIRIN
acetaminophen tablet, film coated |
|
| Product Information |
| Item Code (Source) | NDC: 55670-467 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) | ACETAMINOPHEN | 325 mg |
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| Product Characteristics |
| Color | white (white) | Score | no score |
| Shape | ROUND (ROUND) | Size | 10mm |
| Flavor | | Imprint Code |
AZ;234
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| Contains | |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M013 | 12/30/2008 | |
|
| Part 2 of 9 |
NASAL DECONGESTANT
oxymetazoline hcl spray, metered |
|
| Product Information |
| Item Code (Source) | NDC: 0904-6761 |
| Route of Administration | NASAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) | OXYMETAZOLINE HYDROCHLORIDE | 0.05 g in 100 mL |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| BENZYL ALCOHOL (UNII: LKG8494WBH) | |
| SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74) | |
| EDETATE DISODIUM (UNII: 7FLD91C86K) | |
| MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) | |
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) | |
| SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW) | |
| POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) | |
| POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) | |
| WATER (UNII: 059QF0KO0R) | |
| BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) | |
|
| Product Characteristics |
| Color | white (to off white, viscous) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M012 | 10/12/2018 | |
|
| Part 3 of 9 |
MOORE MEDICAL ANTACID
calcium carbonate tablet, chewable |
|
| Product Information |
| Item Code (Source) | NDC: 55670-142 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) | CALCIUM CARBONATE | 420 mg |
|
|
|
| Product Characteristics |
| Color | white (white) | Score | no score |
| Shape | ROUND (ROUND) | Size | 12mm |
| Flavor | MINT (MINT) | Imprint Code |
FR;8
|
| Contains | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M001 | 12/30/2008 | |
|
| Part 4 of 9 |
MOTION SICKNESS
meclizine hcl tablet |
|
| Product Information |
| Item Code (Source) | NDC: 70677-0026 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570) | MECLIZINE HYDROCHLORIDE | 25 mg |
|
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|
| Product Characteristics |
| Color | yellow | Score | no score |
| Shape | ROUND | Size | 9mm |
| Flavor | | Imprint Code |
44;403
|
| Contains | |
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|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M009 | 06/24/2002 | |
|
| Part 5 of 9 |
AMMONIA INHALANTS
ammonia inhalants inhalant |
|
| Product Information |
| Item Code (Source) | NDC: 46414-3333 |
| Route of Administration | RESPIRATORY (INHALATION) |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) | AMMONIA | 0.045 g in 0.3 mL |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved drug other | | 02/14/1976 | |
|
| Part 6 of 9 |
EASY CARE FIRST AID DIPHENHYDRAMINE
diphenhydramine hydrochloride tablet, film coated |
|
| Product Information |
| Item Code (Source) | NDC: 44224-0017 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) | DIPHENHYDRAMINE HYDROCHLORIDE | 25 mg |
|
|
|
| Product Characteristics |
| Color | pink (pink) | Score | no score |
| Shape | OVAL (OVAL) | Size | 11mm |
| Flavor | | Imprint Code |
048;D
|
| Contains | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M010 | 01/01/2012 | |
|
| Part 7 of 9 |
BZK PADS
benzalkonium chloride swab |
|
| Product Information |
| Item Code (Source) | NDC: 67777-245 |
| Route of Administration | TOPICAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) | BENZALKONIUM CHLORIDE | 1.3 mg in 1 mL |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| WATER (UNII: 059QF0KO0R) | |
|
| Product Characteristics |
| Color | | Score | |
| Shape | RECTANGLE | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M003 | 04/05/2011 | |
|
| Part 8 of 9 |
POVIDONE-IODINE
povidone-iodine solution |
|
| Product Information |
| Item Code (Source) | NDC: 46414-7777 |
| Route of Administration | TOPICAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) | IODINE | 10 mg in 1 mL |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved drug other | | 02/14/1976 | |
|
| Part 9 of 9 |
MOORE MEDICAL BISMUTH
bismuth subsalicylate tablet, chewable |
|
| Product Information |
| Item Code (Source) | NDC: 55670-474 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ, BISMUTH CATION - UNII:ZS9CD1I8YE) | BISMUTH SUBSALICYLATE | 262 mg |
|
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|
| Product Characteristics |
| Color | pink | Score | no score |
| Shape | ROUND | Size | 16mm |
| Flavor | | Imprint Code |
RH;046
|
| Contains | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M008 | 04/01/2014 | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| exempt device | ABC | 01/01/2015 | 10/01/2024 |
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