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ETHYL ALCOHOL by GOJO Industries, Inc.

Dosage form: gel
Ingredients: ALCOHOL 0.70mL in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-967

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
Green Certified
Instant Hand Sanitizer
Kills 99.99% of Germs
renewable

  • USDA BioPreferred product
  • Made with 100% natural renewable ethanol
  • Helps condition skin with a natural moisturizer
  • This product meets the EcoLogoTM environmental standard for instant hand antiseptics based on its use of less intrusive raw materials, a reduction of environmental hazards, and an increase of product recyclability
CCD-170 Certified Instant Hand Antiseptic

Directions
  • Put a small amount in your palm and rub hands together briskly until dry
  • Children under 6 years of age should be supervised when using PURELL

Inactive ingredients
Water (Aqua), Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol



Warnings
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 70% v/v         Antimicrobial

ETHYL ALCOHOL  
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-967
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.70 mL  in 1 mL
Packaging
#Item CodePackage Description
1NDC:21749-967-08236 mL in 1 BOTTLE, PUMP
2NDC:21749-967-12354 mL in 1 BOTTLE, PUMP
3NDC:21749-967-97700 mL in 1 BOTTLE
4NDC:21749-967-891200 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33305/26/2010
Labeler - GOJO Industries, Inc. (004162038)
Registrant - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.004162038manufacture

 
GOJO Industries, Inc.

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Medically reviewed on May 28, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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