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PURELL Advanced Green Certified Instant Hand Sanitizer

Medically reviewed by Drugs.com. Last updated on Jun 24, 2020.

Dosage form: gel
Ingredients: ALCOHOL 0.7mL in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-702

PURELL Advanced Green Certified Instant Hand Sanitizer

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Uses
  • Hand sanitizer to help reduce bacteria on the skin that cause disease
  • Recommended for repeated use

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.

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

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

PURELL ADVANCED GREEN CERTIFIED INSTANT HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-702
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ISOPROPYL ALCOHOL 
CAPRYLYL GLYCOL 
GLYCERIN 
ISOPROPYL MYRISTATE 
.ALPHA.-TOCOPHEROL ACETATE, D- 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
AMINOMETHYLPROPANOL 
Packaging
#Item CodePackage Description
1NDC:21749-702-08237 mL in 1 BOTTLE
2NDC:21749-702-12355 mL in 1 BOTTLE
3NDC:21749-702-97700 mL in 1 BOTTLE
4NDC:21749-702-891200 mL in 1 BOTTLE
5NDC:21749-702-642273 mL in 1 BOTTLE
6NDC:21749-702-101000 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/15/2011
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534MANUFACTURE(21749-702)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.088312414manufacture(21749-702), label(21749-702), pack(21749-702)

 
GOJO Industries, Inc.

Further information

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