PURELL ADVANCED INSTANT HAND SANITIZER- 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 Advanced Instant 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)

Product LabelProduct LabelProduct LabelProduct Label

PURELL ADVANCED INSTANT HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-807
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)  
.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:21749-807-3145 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
2NDC:21749-807-22200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
3NDC:21749-807-23222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
4NDC:21749-807-17515 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/13/2022
5NDC:21749-807-53535 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
6NDC:21749-807-51550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
7NDC:21749-807-331000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
8NDC:21749-807-891200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/11/2011
9NDC:21749-807-97700 mL in 1 PACKAGE; Type 0: Not a Combination Product04/11/2011
10NDC:21749-807-30300 mL in 1 PACKAGE; Type 0: Not a Combination Product08/24/2020
11NDC:21749-807-50189271 mL in 1 PACKAGE; Type 0: Not a Combination Product08/24/2020
12NDC:21749-807-80800 mL in 1 PACKAGE; Type 0: Not a Combination Product02/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/11/2011
Labeler - GOJO Industries, Inc. (004162038)
Registrant - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.036424534manufacture(21749-807)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.088312414manufacture(21749-807) , label(21749-807) , pack(21749-807)

Revised: 5/2022
Document Id: 4a10c193-f5dc-408d-b8f3-07b6fab58944
Set id: 3c3b14e1-4a9d-4ebb-b6b6-ab0173ac06e5
Version: 9
Effective Time: 20220516
 
GOJO Industries, Inc.