PURELL GREEN CERTIFIED INSTANT HAND SANITIZER FOAM (ETHYL ALCOHOL)- alcohol liquid 
GOJO Industries, Inc.

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.

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PURELL Green Certified Instant Hand Sanitizer Foam

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

  • Hand sanitizer to help reduce bacteria on the skin that could 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

  • Put enough product in your palm to cover hands 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, PEG-10 Dimethicone, Glycerin, Hydroxyethyl Urea, Isopropyl Myristate, PEG-12 Dimethicone, Propylene Glycol, Tocopheryl Acetate

Product LabelProduct LabelProduct Label

PURELL GREEN CERTIFIED INSTANT HAND SANITIZER FOAM (ETHYL ALCOHOL) 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-987
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.70 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21749-987-53535 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/15/201011/30/2023
2NDC:21749-987-51550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/15/201011/30/2023
3NDC:21749-987-97700 mL in 1 BOTTLE; Type 0: Not a Combination Product12/15/201011/30/2023
4NDC:21749-987-101000 mL in 1 BOTTLE; Type 0: Not a Combination Product12/15/201011/30/2023
5NDC:21749-987-891200 mL in 1 BOTTLE; Type 0: Not a Combination Product12/15/201011/30/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/15/201011/30/2023
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.088312414label(21749-987) , pack(21749-987) , manufacture(21749-987)

Revised: 3/2021
Document Id: 796ad152-9e0e-43bb-95ba-f35c91385577
Set id: 5b9191e0-da0f-47e6-9d8a-5cd6637bd2b3
Version: 6
Effective Time: 20210329
 
GOJO Industries, Inc.