Skip to main content

Purell Advanced Refreshing Aloe

Dosage form: gel
Ingredients: ALCOHOL 0.7mL in 1mL
Labeler: GOJO Industries, Inc.
NDC code: 21749-705

Medically reviewed by Drugs.com. Last updated on Dec 23, 2024.

PURELL Advanced Hand Sanitizer Refreshing Aloe

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Uses
  • Hand sanitizer to help reduce bacteria on the skin

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
  • Put enough product in your palm to cover hands and rub hands together briskly until dry
  • Children under 6 years of age should be supervised when using PURELL

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.

PURELL ADVANCED REFRESHING ALOE 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-705
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ISOPROPYL ALCOHOL 
ALOE VERA LEAF 
CAPRYLYL GLYCOL 
GLYCERIN 
ISOPROPYL MYRISTATE 
.ALPHA.-TOCOPHEROL ACETATE, D- 
AMINOMETHYLPROPANOL 
FD&C BLUE NO. 1 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:21749-705-5015 mL in 1 PACKAGE
2NDC:21749-705-0130 mL in 1 PACKAGE
3NDC:21749-705-0259 mL in 1 BOTTLE
4NDC:21749-705-04118 mL in 1 PACKAGE
5NDC:21749-705-08236 mL in 1 BOTTLE
6NDC:21749-705-10295 mL in 1 PACKAGE
7NDC:21749-705-12354 mL in 1 BOTTLE
8NDC:21749-705-20591 mL in 1 PACKAGE
9NDC:21749-705-80800 mL in 1 PACKAGE
10NDC:21749-705-331000 mL in 1 PACKAGE
11NDC:21749-705-891200 mL in 1 PACKAGE
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/FEIOperations
GOJO Industries, Inc.036424534MANUFACTURE(21749-705)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.088312414MANUFACTURE(21749-705), label(21749-705), pack(21749-705)

Revised: 01/2022
Document Id: 673d90bd-dab5-45ba-ae59-127e583a0edb
Set id: 3330c320-49f3-4dd0-a1bd-39c1f9632370
Version: 4
Effective Time: 20220101
 
GOJO Industries, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer