PURELL INSTANT HAND SANITIZER FOAM (ETHYL ALCOHOL)- alcohol gel 
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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Active Ingredient

Ethyl alcohol 62%

Use

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

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.

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

Purpose

Antimicrobial

Inactive Ingredients

Water (Aqua), Isopropyl Alcohol, PEG-10 Dimethicone, Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Fragrance (Parfum)

Product Label
Product Label
PURELL INSTANT HAND SANITIZER FOAM (ETHYL ALCOHOL) 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-515
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 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:21749-515-3145 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/14/2010
2NDC:21749-515-53535 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/14/2010
3NDC:21749-515-51550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/14/2010
4NDC:21749-515-331000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/14/2010
5NDC:21749-515-891200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/14/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/14/201001/01/2020
Labeler - GOJO Industries, Inc. (004162038)

Revised: 11/2018
Document Id: 3a4fcccf-f49a-43f4-8ee8-06fbcc399270
Set id: b5bae1e7-2ee2-48e6-a50a-194527a19d39
Version: 3
Effective Time: 20181119
 
GOJO Industries, Inc.