MODEL AA-1218CEV
first aid kit with drug kit |
| Product Information |
| Product Type | MEDICAL DEVICE | Item Code (Source) | NHRIC:27860-010 |
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| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NHRIC:27860-010-11 | 1 in 1 PACKAGE; Type 1: Convenience Kit of Co-Package | | |
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| 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 10 | | 1 |
| Part 11 | | 1 |
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| Part 1 of 11 |
MOORE MEDICAL NON ASPIRIN
acetaminophen tablet, film coated |
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| Product Information |
| Item Code (Source) | NDC: 55670-467 |
| Route of Administration | ORAL |
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| 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 11 |
MOORE MEDICAL ANTACID
calcium carbonate tablet, chewable |
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| Product Information |
| Item Code (Source) | NDC: 55670-142 |
| Route of Administration | ORAL |
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| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) | CALCIUM CARBONATE | 420 mg |
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| Product Characteristics |
| Color | white (white) | Score | no score |
| Shape | ROUND (ROUND) | Size | 12mm |
| Flavor | MINT (MINT) | Imprint Code |
FR;8
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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 | M001 | 12/30/2008 | |
|
| Part 3 of 11 |
AMMONIA INHALANTS
ammonia inhalants inhalant |
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| Product Information |
| Item Code (Source) | NDC: 46414-3333 |
| Route of Administration | RESPIRATORY (INHALATION) |
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| 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 4 of 11 |
EASY CARE FIRST AID DIPHENHYDRAMINE
diphenhydramine hydrochloride tablet, film coated |
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| 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 |
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| Product Characteristics |
| Color | pink (pink) | Score | no score |
| Shape | OVAL (OVAL) | Size | 11mm |
| Flavor | | Imprint Code |
048;D
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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 | M010 | 01/01/2012 | |
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| Part 5 of 11 |
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 |
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| Inactive Ingredients |
| Ingredient Name | Strength |
| WATER (UNII: 059QF0KO0R) | |
|
| Product Characteristics |
| Color | | Score | |
| Shape | RECTANGLE | Size | |
| Flavor | | Imprint Code | |
| Contains | |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M003 | 04/05/2011 | |
|
| Part 6 of 11 |
POVIDONE-IODINE
povidone-iodine solution |
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| 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 7 of 11 |
MOORE MEDICAL BISMUTH
bismuth subsalicylate tablet, chewable |
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| 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 | |
|
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M008 | 04/01/2014 | |
|
| Part 8 of 11 |
MOOREBRAND PHENYLEPHRINE
phenylephrine hydrochloride tablet, film coated |
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| Product Information |
| Item Code (Source) | NDC: 55670-163 |
| Route of Administration | ORAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) | PHENYLEPHRINE HYDROCHLORIDE | 5 mg |
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| Product Characteristics |
| Color | red (red) | Score | no score |
| Shape | ROUND (ROUND) | Size | 7mm |
| Flavor | | Imprint Code |
271
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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 | M012 | 12/30/2008 | |
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| Part 9 of 11 |
STYE
mineral oil and petrolatum gel |
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| Product Information |
| Item Code (Source) | NDC: 63736-238 |
| Route of Administration | OPHTHALMIC |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) | MINERAL OIL | 319 mg in 1 g |
| PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) | PETROLATUM | 577 mg in 1 g |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) | |
| STEARIC ACID (UNII: 4ELV7Z65AP) | |
| WHEAT GERM OIL (UNII: 14C97E680P) | |
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| Product Characteristics |
| Color | white (Clear) | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M018 | 06/15/2010 | |
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| Part 10 of 11 |
ANTIMICROBIAL
alcohol liquid |
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| Product Information |
| Item Code (Source) | NDC: 61010-3111 |
| Route of Administration | TOPICAL |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) | alcohol | 665 mL in 1 L |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC Monograph Drug | M003 | 05/21/2012 | |
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| Part 11 of 11 |
PHYSICIANSCARE OPHTHALMIC SOLUTION EYEWASH
purified water 98.3% solution |
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| Product Information |
| Item Code (Source) | NDC: 0924-0160(NDC: 65785-160) |
| Route of Administration | OPHTHALMIC |
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| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) | WATER | 929 g in 946 mL |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| NDA | NDA022305 | 06/12/2013 | |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| exempt device | ABC | 01/01/2015 | 10/25/2024 |
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