PURELL HEALTHCARE ADVANCED HAND SANITIZER FOAM- alcohol liquid 
GOJO Industries, Inc.

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PURELL Healthcare 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 ifirritation 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 110 oF (43 oC)

May discolor certain fabrics or surfaces

Inactive ingredients

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

Product Label

PURELL HEALTHCARE ADVANCED HAND SANITIZER FOAM 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-811
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21749-811-45450 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/201801/31/2022
2NDC:21749-811-53535 mL in 1 PACKAGE; Type 0: Not a Combination Product09/05/201710/31/2026
3NDC:21749-811-891200 mL in 1 PACKAGE; Type 0: Not a Combination Product09/05/2017
4NDC:21749-811-80800 mL in 1 PACKAGE; Type 0: Not a Combination Product06/05/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/05/2017
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.036424534manufacture(21749-811)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.088312414manufacture(21749-811) , label(21749-811) , pack(21749-811)

Revised: 12/2024
Document Id: 2964dd4f-0f62-3168-e063-6294a90a7125
Set id: d7f06d27-bc15-434f-8572-cd916d9924b2
Version: 5
Effective Time: 20241216
 
GOJO Industries, Inc.