PURELL ADVANCED SOOTHING- 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 Soothing 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

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Blue 1 (CI 42090), Yellow 5 (CI 19140)

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.

Product LabelProduct LabelProduct LabelProduct Label

PURELL ADVANCED SOOTHING 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-713
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)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21749-713-0130 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
2NDC:21749-713-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2018
3NDC:21749-713-04118 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
4NDC:21749-713-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2018
5NDC:21749-713-10295 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
6NDC:21749-713-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2018
7NDC:21749-713-20591 mL in 1 PACKAGE; Type 1: Convenience Kit of Co-Package11/01/2018
8NDC:21749-713-27800 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
9NDC:21749-713-28826 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
10NDC:21749-713-331000 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
11NDC:21749-713-401200 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
12NDC:21749-713-672000 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
13NDC:21749-713-65192 mL in 1 PACKAGE; Type 0: Not a Combination Product07/01/2021
14NDC:21749-713-24710 mL in 1 PACKAGE; Type 0: Not a Combination Product08/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/01/2018
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.036424534MANUFACTURE(21749-713)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.088312414MANUFACTURE(21749-713) , label(21749-713) , pack(21749-713)

Revised: 12/2022
Document Id: 535b90bd-11f8-4323-baaa-b40709ba4637
Set id: 59b47629-8b4e-4084-8bc8-66c7e5599e9c
Version: 6
Effective Time: 20221216
 
GOJO Industries, Inc.