PURE FOAM- alcohol aerosol, foam

Pure Foam by

Drug Labeling and Warnings

Pure Foam by is a Otc medication manufactured, distributed, or labeled by Phoenix Research Industries, Inc., ABC Compounding Co., Inc., ABC Compounding Company of Texas, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Box OTC-Active Ingredients Section

Ethyl Alcohol 62%

Drug Facts Box OTC-Purpose Section

Antiseptic

Drug Facts Box OTC-Indications and Usage Section

for hand-washing to decrease bacteria on the skin, only when water is not available

Drug Facts Box OTC-Warnings Section

Flammable, keep away from fire and flames

For external use only

Drug Facts Box OTC-When Using Section

do not get into eyes

if contact occurs, rinse eyes thoroughly with water

Drug Facts Box OTC-Stop Use Section

irritation and redness develop

Drug Facts Box OTC-Keep Out of Reach of Children Section

If swallowed, get medical help or contact a Poison Control Center right away

Drug Facts Box OTC-Dosage & Administration Section

press valve once to deliver one squirt (about a quarter size) of foaming product onto the palm of your hand

rub hands together and allow to dry without wiping

Drug Facts Box OTC-Inactive Ingredients Section

water, DEA-C8-18 perfluoroalkylethyl phosphate, cetearyl alcohol, polysorbate 65, dimethicone PEG-8 meadowfoamate, meadowfoamamidopropyl betaine, butane, propane, fragrance

Pure Foam 4773 454g

477320F10010.jpg  Pure Foam 454g

INGREDIENTS AND APPEARANCE

PURE FOAM 
alcohol aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50452-773
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	620 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PROPANE (UNII: T75W9911L6)
BUTANE (UNII: 6LV4FOR43R)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50452-773-25	199 g in 1 CAN
2	NDC: 50452-773-26	454 g in 1 CAN

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	01/31/2010

Labeler - Phoenix Research Industries, Inc. (152259904)

Registrant - ABC Compounding Co., Inc. (003284353)

Establishment
Name	Address	ID/FEI	Business Operations
ABC Compounding Company of Texas, Inc.		026219253	manufacture