PURELL ADVANCED REFRESHING - 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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PURELL Advanced Hand Sanitizer Refreshing Gel

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Uses

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

Other information

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum)

Distributed by:
GOJO Industries, Inc.
Akron, OH 44309
Questions?
Tel: 1-888-4-PURELL
www.PURELL.com
©2011.
GOJO Industries, Inc.
All rights reserved.
Made in U.S.A.

Package/Label Principal Display Panel

Bottle Label

PURELL ADVANCED REFRESHING 
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-704
Route of Administration TOPICAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:21749-704-01 29 mL in 1 BOTTLE; Type 0: Not a Combination Product
2 NDC:21749-704-02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product
3 NDC:21749-704-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product
4 NDC:21749-704-12 354 mL in 1 BOTTLE; Type 0: Not a Combination Product
5 NDC:21749-704-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product
6 NDC:21749-704-10 295 mL in 1 PACKAGE; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 03/15/2012
Labeler - GOJO Industries, Inc. (004162038)
Establishment
Name Address ID/FEI Business Operations
GOJO Industries, Inc. 036424534 MANUFACTURE(21749-704)

Revised: 2/2016
Document Id: da9d134e-3353-43a3-8832-37dc2d6b4b83
Set id: b1beadc4-5cf4-4e28-90cc-3f9fdc132a90
Version: 4
Effective Time: 20160201
 
GOJO Industries, Inc.