Pharmacys Prescription IPA: Package Insert and Label Information

PHARMACYS PRESCRIPTION IPA- isopropyl alcohol liquid
American Consumer Products Corp

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.

Active Ingredient (by volume)

Isopropyl alcohol (70% conc.)



First Aid Antiseptic


Uses: first aid to help prevent the risk of infection in minor cuts, scrapes, burns



For external use only

If taken internally serious gastric disturbances will result

Flammable ​• keep away from fire or flame, heat, spark, electrical

When using this product

When using this product • do not get into eyes • do not inhale • do not apply over large area of the body • do not use longer than 1 week

Stop use

Stop use and ask a doctor if condition persists or gets worse

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


Caution — Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into eyes or mucus membranes. Avoid inhaling this product.


Directions • clean the affected area • apply a small amount of this product on the area 1 to 2 times daily • may be covered with a sterile bandage • if bandaged, let dry first

Other information

Other information • does not contain, nor is intended as a substitute for grain or ethyl alcohol.

Inactive ingredient

Inactive ingredient Water (Aqua)

Tamper Evident

Tamper Evident: Do Not Use if the under cap safety foil is broken or missing.

Distributed by

Distributed by:

American Consumer Products Corp

Vernon, CA 90058

Principal Display Panel

Pharmacys Prescription Isopropyl Alcohol
(click image for full-size original)

isopropyl alcohol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:72197-036
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Inactive Ingredients
Ingredient Name Strength
# Item Code Package Description Multilevel Packaging
1 NDC:72197-036-12 354.8 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 09/14/2020
Labeler — American Consumer Products Corp (081101181)

Revised: 09/2020 American Consumer Products Corp provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

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