First Aid Only Instant Hand Sanitizer Gel

First Aid Only Instant Hand Sanitizer by

Drug Labeling and Warnings

First Aid Only Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FIRST AID ONLY INSTANT HAND SANITIZER- alcohol gel 
Acme United Corporation

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First Aid Only Instant Hand Sanitizer Gel

Active Ingredient(s)

Ethyl Alcohol 70% w/w

Purpose

Antimicrobial

Use

.hand sanitizer to help reduce microbes on the skin

Warnings

Flammable. Keep away from fire or flame For external use only

When using this product, do not use in or near the eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

put enough gel in your palm to cover your hands and rub hand together rapidly until dry

■ children under 6 years of age should be supervised when using this product

Other information

■ store below 110°F {43°C)

■ may discolor certain fabrics or surfaces

Inactive ingredients

carbomer, fragrance, glycerin, propylene glycol, silicone, triethanolamine, water (aqua)

Package Label - Principal Display Panel

60 mL NDC: 0924-0401-01

FIRST AID ONLY INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-0401(NDC: 28691-0700)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	77 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SILICON (UNII: Z4152N8IUI)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-0401-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/09/2020
2	NDC: 0924-0401-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/09/2020
3	NDC: 0924-0401-03	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/09/2020
4	NDC: 0924-0401-04	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/09/2020
5	NDC: 0924-0401-05	750 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/09/2020
6	NDC: 0924-0401-06	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/09/2020	02/28/2022

Labeler - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		045924339	relabel(0924-0401) , repack(0924-0401)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		080119599	relabel(0924-0401) , repack(0924-0401)

Revised: 10/2024

Document Id: 2511e329-6efd-7199-e063-6394a90ac374

34390-5

Set id: a7a8a84d-d0ee-2881-e053-2a95a90a59c4

Version: 2

Effective Time: 20241022