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PURELL Professional Advanced Hand Sanitizer Foam

Medically reviewed on Sep 5, 2017

Dosage form: liquid
Ingredients: ALCOHOL 0.70mL in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-810

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 Professional Advanced Hand Sanitizer Foam

Active ingredient

Ethyl Alcohol 70%

Purpose

Antimicrobial

Use

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

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. 

Rub hands together briskly until dry.

Children under 6 years of age should be supervised when using this product.

Other information

Store below 110oF (43oC)

May discolor certain fabrics or surfaces

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Fragrance (Parfum)

PURELL PROFESSIONAL ADVANCED HAND SANITIZER FOAM 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-810
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.70 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Isopropyl Alcohol 
Glycerin 
Isopropyl Myristate 
.ALPHA.-TOCOPHEROL ACETATE, D- 
Caprylyl Glycol 
PEG-12 DIMETHICONE (300 CST) 
Packaging
#Item CodePackage Description
1NDC:21749-810-53535 mL in 1 PACKAGE
2NDC:21749-810-891200 mL in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/05/2017
Labeler - GOJO Industries, Inc. (004162038)
Registrant - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534manufacture(21749-810)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.088312414manufacture(21749-810), label(21749-810), pack(21749-810)

 
GOJO Industries, Inc.

Further information

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

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