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Pure Foam

Phoenix Research Industries, Inc.
ABC Compounding Co., Inc.

Pure Foam 4773 Drug Facts and Label


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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 454gPure Foam

Pure Foam

ALCOHOL AEROSOL, FOAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50452-773
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 620 mg

Inactive Ingredients

Ingredient Name Strength
propane
BUTANE
water

Packaging

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

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part333 2010-01-31


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