PHARMACYS PRESCRIPTION RUBBING ALCOHOL- alcohol liquid

Pharmacys Prescription Rubbing Alcohol by

Drug Labeling and Warnings

Pharmacys Prescription Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by American Consumer Products Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient (by volume)

Isopropyl alcohol (50% conc.)

Purpose

Purpose

Antiseptic

Uses

Uses
● helps reduce bacteria and germs on skin.
● helps relieve minor muscular aches due to exertion.

Warnings

Warnings

For external use only

● flammable, keep away from fire or flame

● not recommended for deep puncture wounds, animal bites or serious burns

● if taken internally, serious gastric disturbances will result

When using this product

When using this product ● do not get into eyes ● do not apply over large areas of
the body ● do not use longer than one week.

Stop use

Stop use if ● condition persists or gets worse

Keep out of reach of children

Keep out of reach of children. Do not use on children less than 2 months of age.
Supervise use in children under 6 years of age to prevent accidental swallowing.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions ●clean skin and apply a small amount of this product 1-3 times daily on a selected area as needed ● allow product to remain on skin surface until dry

Inactive ingredient

Inactive ingredient: purified water (Aqua)

Pharmacys Prescription Isopropyl Rubbing Alcohol

INGREDIENTS AND APPEARANCE

PHARMACYS PRESCRIPTION RUBBING ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	50 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-030-11	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/02/2020

Labeler - American Consumer Products Corp (081101181)