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PURELL Advanced Instant Hand Sanitizer

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

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

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-700
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.70 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Isopropyl Alcohol 
Glycerin 
Isopropyl Myristate 
.ALPHA.-TOCOPHEROL ACETATE, D- 
Caprylyl Glycol 
AMINOMETHYLPROPANOL 
Packaging
#Item CodePackage Description
1NDC:21749-700-0224 BOTTLE in 1 CASE
159 mL in 1 BOTTLE
2NDC:21749-700-108 BAG in 1 CASE
21000 mL in 1 BAG
3NDC:21749-700-894 BOTTLE in 1 CASE
31200 mL in 1 BOTTLE
4NDC:21749-700-204 BAG in 1 CASE
42000 mL in 1 BAG
5NDC:21749-700-674 BOTTLE, PUMP in 1 CASE
52000 mL in 1 BOTTLE, PUMP
6NDC:21749-700-04118 mL in 1 BOTTLE
7NDC:21749-700-80800 mL in 1 BOTTLE
8NDC:21749-700-12355 mL in 1 BOTTLE
9NDC:21749-700-07222 mL in 1 BOTTLE
10NDC:21749-700-0130 mL in 1 BOTTLE
11NDC:21749-700-59590 mL in 1 BOTTLE
12NDC:21749-700-1515 mL in 1 BOTTLE
13NDC:21749-700-6060 mL in 1 BOTTLE
14NDC:21749-700-47473 mL in 1 BOTTLE
15NDC:21749-700-0389 mL in 1 BOTTLE
16NDC:21749-700-08236 mL in 1 BOTTLE
17NDC:21749-700-001.2 mL in 1 BOTTLE
18NDC:21749-700-45450 mL in 1 PACKAGE
19NDC:21749-700-29295 mL in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/10/2011
Labeler - GOJO Industries, Inc. (004162038)
Registrant - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534manufacture(21749-700)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.088312414manufacture(21749-700), label(21749-700), pack(21749-700)
Establishment
NameAddressID/FEIOperations
Travis Association for the Blind026032268pack(21749-700)

 
GOJO Industries, Inc.

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Medically reviewed on Dec 5, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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