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Purell Alcohol Formulation

Dosage form: swab
Ingredients: ALCOHOL 0.62mL in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-367

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 Hand Sanitizing Wipes Alcohol Formulation

Active ingredient

Ethyl alcohol 62%

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 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

• Wet hands thoroughly with product and allow to dry

• Children under 6 years of age should be supervised when using PURELL® products

Other information

• Store below 110°F (43°C)

• May discolor certain fabrics or surfaces

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Propylene Glycol, Retinyl Palmitate, Tocopheryl Acetate, Zea Mays (Corn) Oil

Label

PURELL ALCOHOL FORMULATION 
alcohol swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-367
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.62 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ISOPROPYL ALCOHOL 
GLYCERIN 
ALOE VERA LEAF 
ISOPROPYL MYRISTATE 
PROPYLENE GLYCOL 
VITAMIN A PALMITATE 
.ALPHA.-TOCOPHEROL ACETATE 
CORN OIL 
Packaging
#Item CodePackage Description
1NDC:21749-367-764 mL in 1 POUCH
2NDC:21749-367-2496 mL in 1 PACKAGE
3NDC:21749-367-36144 mL in 1 PACKAGE
4NDC:21749-367-63315 mL in 1 CANISTER
5NDC:21749-367-94540 mL in 1 PACKAGE
6NDC:21749-367-68700 mL in 1 CANISTER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/24/2012
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534manufacture(21749-367)

Revised: 06/2016
 
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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