PURELL Advanced Green Certified Instant Hand Sanitizer

Dosage form: gel
Ingredients: ALCOHOL 0.7mL in 1mL
Labeler: GOJO Industries, Inc.
NDC code: 21749-702

Medically reviewed by Drugs.com. Last updated on Jun 14, 2023.

PURELL Advanced Green Certified Instant Hand Sanitizer

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on the skin that cause disease
Recommended for repeated use

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

Place enough product in your palm to thoroughly cover your hands
Run hands together briskly until dry
Children under 6 years of age should be supervised when using this product.

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

PURELL ADVANCED GREEN CERTIFIED INSTANT HAND SANITIZER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-702
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (ALCOHOL)	ALCOHOL	0.7 mL in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER
ISOPROPYL ALCOHOL
CAPRYLYL GLYCOL
GLYCERIN
ISOPROPYL MYRISTATE
.ALPHA.-TOCOPHEROL ACETATE, D-
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
AMINOMETHYLPROPANOL

Packaging
#	Item Code	Package Description
1	NDC:21749-702-08	237 mL in 1 BOTTLE
2	NDC:21749-702-12	355 mL in 1 BOTTLE
3	NDC:21749-702-97	700 mL in 1 BOTTLE
4	NDC:21749-702-89	1200 mL in 1 BOTTLE
5	NDC:21749-702-64	2273 mL in 1 BOTTLE
6	NDC:21749-702-10	1000 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/15/2011

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Operations
GOJO Industries, Inc.		036424534	MANUFACTURE(21749-702)

Establishment
Name	Address	ID/FEI	Operations
GOJO Industries, Inc.		088312414	manufacture(21749-702), label(21749-702), pack(21749-702)

Document Id: 9891b826-9632-4e58-9633-e63a4d00d878

Set id: bd308bd4-d38f-4e48-ae52-49ec30c752d5

Version: 7

Effective Time: 20200624

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

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