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Purell Advanced Hand Sanitizer Refreshing Florals

Dosage form: gel
Ingredients: ALCOHOL 0.7mL in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-146

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 Florals

Active Ingredients

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Use

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 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

Place enough product in your palm to thoroughly cover your hands

Rub hands together briskly until dry

Children under 6 years of age should be supervised when using this product

Other information

Store below 110°F (43°C)

May discolor certain fabrics or surfaces

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Caprylyl glycol, Glycerin, Isopropyl Myristate, Lactose, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Cellulose, Hydroxypropyl Methylcellulose, Fragrance (Parfum), Red 33 (CI 17200), Red 40 (CI 16035), Ultramarines (CI 77007)

Package/Label Principal Display Panel

Purell Advanced Hand Sanitizer Refreshing Florals

Kills the Most Germs* *Ounce for ounce kills outperforms PURELL Original formulations when used on hands as directed

Kills more than 99.99% of most common germs that may make you sick


Distributed by:

GOJO Industries, Inc.

Akron, OH 44309

Questions? Tel: 1-888-4-PURELL www.PURELL.com

(C) 2012. GOJO Industries, Inc.

All rights reserved. Made in U.S.A.


Patent Pending

PURELL ADVANCED HAND SANITIZER REFRESHING FLORALS  
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-146
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 
CAPRYLYL GLYCOL 
GLYCERIN 
ISOPROPYL MYRISTATE 
LACTOSE 
.ALPHA.-TOCOPHEROL ACETATE 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
AMINOMETHYLPROPANOL 
POWDERED CELLULOSE 
HYPROMELLOSES 
D&C RED NO. 33 
FD&C RED NO. 40 
ULTRAMARINE BLUE 
Packaging
#Item CodePackage Description
1NDC:21749-146-0130 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/01/2012
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534manufacture(21749-146)

Revised: 11/2012
 
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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