PURELL ADVANCED SKIN NOURISHING INSTANT HAND SANITIZER- alcohol liquid

PURELL Advanced Skin Nourishing Instant Hand Sanitizer by

Drug Labeling and Warnings

PURELL Advanced Skin Nourishing Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by GOJO Industries, Inc., Travis Association for the Blind. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin that could 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
• 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, Glycerin, Caprylyl glycol, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELL ADVANCED SKIN NOURISHING INSTANT HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-701
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.70 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Isopropyl Alcohol (UNII: ND2M416302)
Glycerin (UNII: PDC6A3C0OX)
Isopropyl Myristate (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
Caprylyl Glycol (UNII: 00YIU5438U)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-701-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2012
2	NDC: 21749-701-10	1000 mL in 1 BAG; Type 0: Not a Combination Product	06/01/2012
3	NDC: 21749-701-89	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2012
4	NDC: 21749-701-12	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/01/2012

Labeler - GOJO Industries, Inc. (004162038)

Registrant - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	manufacture(21749-701)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		088312414	manufacture(21749-701) , label(21749-701) , pack(21749-701)

Establishment
Name	Address	ID/FEI	Business Operations
Travis Association for the Blind		026032268	label(21749-701) , repack(21749-701)