PURELL GREEN CERTIFIED INSTANT HAND SANITIZER FOAM (ETHYL ALCOHOL)- alcohol liquid

PURELL Green Certified Instant Hand Sanitizer Foam (ETHYL ALCOHOL) by

Drug Labeling and Warnings

PURELL Green Certified Instant Hand Sanitizer Foam (ETHYL ALCOHOL) by is a Otc medication manufactured, distributed, or labeled by GOJO Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

• 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

• Put enough product in your palm to cover hands and rub hands together briskly until dry
• Children under 6 years of age should be supervised when using PURELL

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, PEG-10 Dimethicone, Glycerin, Hydroxyethyl Urea, Isopropyl Myristate, PEG-12 Dimethicone, Propylene Glycol, Tocopheryl Acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELL GREEN CERTIFIED INSTANT HAND SANITIZER FOAM (ETHYL ALCOHOL) 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-987
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)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-987-53	535 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/15/2010
2	NDC: 21749-987-51	550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/15/2010
3	NDC: 21749-987-97	700 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/15/2010
4	NDC: 21749-987-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/15/2010
5	NDC: 21749-987-89	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/15/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/15/2010

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		088312414	label(21749-987) , pack(21749-987) , manufacture(21749-987)