PURELL ADVANCED REFRESHING ALOE- 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 Aloe

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 Label

PURELL ADVANCED REFRESHING ALOE 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-705
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:21749-705-5015 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
2NDC:21749-705-0130 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
3NDC:21749-705-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product03/14/201201/01/2022
4NDC:21749-705-04118 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
5NDC:21749-705-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product03/14/201201/01/2022
6NDC:21749-705-10295 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
7NDC:21749-705-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product03/14/201201/01/2022
8NDC:21749-705-20591 mL in 1 PACKAGE; Type 1: Convenience Kit of Co-Package03/14/201201/01/2022
9NDC:21749-705-80800 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
10NDC:21749-705-331000 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
11NDC:21749-705-891200 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/14/201201/01/2022
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.036424534MANUFACTURE(21749-705)
Establishment
NameAddressID/FEIBusiness Operations
GOJO Industries, Inc.088312414MANUFACTURE(21749-705) , label(21749-705) , pack(21749-705)

Revised: 1/2022
Document Id: 673d90bd-dab5-45ba-ae59-127e583a0edb
Set id: 3330c320-49f3-4dd0-a1bd-39c1f9632370
Version: 4
Effective Time: 20220101
 
GOJO Industries, Inc.