GERMIFREE ANTIMICROBIAL HAND GEL- ethyl alcohol gel 
Acme United Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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GermiFree Antimicrobial Hand Gel

Drug Facts

Active ingredient

Ethyl alcohol 60% 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 and continues

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 hands and rub hands 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)

Kill Germs up to 99.99% of most common germs that may cause illness

Distributed by:

Acme United Corporation

55 Walls Drive

Fairfield, CT 06824

1-800-835-2263

Made in Egypt

Packaging

Germfr60

GERMIFREE ANTIMICROBIAL HAND GEL 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0400(NDC:28691-6000)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL67.7 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SILICON (UNII: Z4152N8IUI)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0924-0400-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product06/11/2020
2NDC:0924-0400-02100 mL in 1 BOTTLE; Type 0: Not a Combination Product06/11/2020
3NDC:0924-0400-03200 mL in 1 BOTTLE; Type 0: Not a Combination Product06/11/2020
4NDC:0924-0400-04500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/11/2020
5NDC:0924-0400-05750 mL in 1 BOTTLE; Type 0: Not a Combination Product06/11/2020
6NDC:0924-0400-061000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/11/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/11/2020
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation045924339relabel(0924-0400) , repack(0924-0400)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation080119599relabel(0924-0400) , repack(0924-0400)

Revised: 6/2020
Document Id: a7d6a7ae-2216-05d0-e053-2995a90ad06a
Set id: a7d6a792-5ad6-cfa2-e053-2995a90ad4f2
Version: 1
Effective Time: 20200610
 
Acme United Corporation