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ETHYL ALCOHOL by GOJO Industries, Inc.

Dosage form: gel
Ingredients: ALCOHOL 0.62mL in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-965

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.

Purell Instant Hand Sanitizer
Kills 99.99% of Germs

Place enough product in your palm to thoroughly cover your hands
Rub hands together briskly until dry
Children under 6 years of age should be supervised when using this product.

Hand sanitizer to help reduce bacteria on the skin that could cause disease

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

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and lasts
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Active ingredient                            Purpose

Ethyl alcohol 62%                              Antimicrobial

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Diisopropyl Sebacate, Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Aminomethyl Propanol, Carbomer, Fragrance (Parfum)

alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-965
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
#Item CodePackage Description
1NDC:21749-965-80800 mL in 1 BOX
2NDC:21749-965-202000 mL in 1 BOX
3NDC:21749-965-0515 mL in 1 BOTTLE
4NDC:21749-965-0259 mL in 1 BOTTLE
5NDC:21749-965-04118 mL in 1 BOTTLE
6NDC:21749-965-08236 mL in 1 BOTTLE, PUMP
7NDC:21749-965-12354 mL in 1 BOTTLE, PUMP
8NDC:21749-965-59591 mL in 1 BOTTLE, PUMP
9NDC:21749-965-672000 mL in 1 BOTTLE, PUMP
10NDC:21749-965-101000 mL in 1 BOX
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33303/15/2010
Labeler - GOJO Industries, Inc. (004162038)
Registrant - GOJO Industries, Inc. (004162038)
GOJO Industries, Inc.004162038manufacture

GOJO Industries, Inc.

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Medically reviewed on Mar 16, 2018

Further information

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