Purell Advanced Refreshing Aloe

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

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.

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

Other information
  • Store below 110°F (43°C)
  • May discolor certain fabrics or surfaces

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.

Package/Label Principal Display Panel

New!
More Effective Formula

Purell 
ADAVANCED
Hand Sanitizer

KILLS THE MOST GERMS

Refreshing Aloe

Kills More Than 99.99% of Germs
Leaves Hands Feeling Soft

8 FL OZ (236 mL)

Bottle Label

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:21749-705-0259 mL in 1 BOTTLE
2NDC:21749-705-08236 mL in 1 BOTTLE
3NDC:21749-705-12354 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/14/2012
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534MANUFACTURE(21749-705)

Revised: 04/2012
 
GOJO Industries, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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