PURELL Advanced Instant Hand Sanitizer

Dosage form: liquid
Ingredients: ALCOHOL 0.70mL in 1mL
Labeler: GOJO Industries, Inc.
NDC code: 21749-700

Medically reviewed by Drugs.com. Last updated on Dec 17, 2024.

PURELL Advanced Hand Sanitizer

Active ingredient

Ethyl alcohol 70%

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin that could cause disease

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

Rub hands together briskly until dry

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

Inactive ingredients

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

PURELL ADVANCED INSTANT HAND SANITIZER
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-700
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (ALCOHOL)	ALCOHOL	0.70 mL in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water
Isopropyl Alcohol
Glycerin
Isopropyl Myristate
.ALPHA.-TOCOPHEROL ACETATE, D-
Caprylyl Glycol
AMINOMETHYLPROPANOL

Packaging
#	Item Code	Package Description
1	NDC:21749-700-02	24 BOTTLE in 1 CASE
1		59 mL in 1 BOTTLE
2	NDC:21749-700-10	8 BAG in 1 CASE
2		1000 mL in 1 BAG
3	NDC:21749-700-89	4 BOTTLE in 1 CASE
3		1200 mL in 1 BOTTLE
4	NDC:21749-700-20	4 BAG in 1 CASE
4		2000 mL in 1 BAG
5	NDC:21749-700-67	4 BOTTLE, PUMP in 1 CASE
5		2000 mL in 1 BOTTLE, PUMP
6	NDC:21749-700-04	118 mL in 1 BOTTLE
7	NDC:21749-700-80	800 mL in 1 BOTTLE
8	NDC:21749-700-12	355 mL in 1 BOTTLE
9	NDC:21749-700-07	222 mL in 1 BOTTLE
10	NDC:21749-700-01	30 mL in 1 BOTTLE
11	NDC:21749-700-59	590 mL in 1 BOTTLE
12	NDC:21749-700-15	15 mL in 1 BOTTLE
13	NDC:21749-700-60	60 mL in 1 BOTTLE
14	NDC:21749-700-47	473 mL in 1 BOTTLE
15	NDC:21749-700-03	89 mL in 1 BOTTLE
16	NDC:21749-700-08	236 mL in 1 BOTTLE
17	NDC:21749-700-00	1.2 mL in 1 BOTTLE
18	NDC:21749-700-45	450 mL in 1 PACKAGE
19	NDC:21749-700-29	295 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/10/2011

Labeler - GOJO Industries, Inc. (004162038)

Registrant - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Operations
GOJO Industries, Inc.		036424534	manufacture(21749-700)

Establishment
Name	Address	ID/FEI	Operations
GOJO Industries, Inc.		088312414	manufacture(21749-700), label(21749-700), pack(21749-700)

Establishment
Name	Address	ID/FEI	Operations
Travis Association for the Blind		026032268	pack(21749-700)

Revised: 12/2019

Document Id: 4425cddd-a21d-42b2-acd4-31728a315c36

Set id: 49bce138-8be2-4bf4-9eeb-f354308cd594

Version: 12

Effective Time: 20191227

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