Active Ingredient
Active Ingredient (by volume)
Isopropyl alcohol (50% conc.)
Pharmacys Prescription Rubbing Alcohol
FDA Label NDC 72197-030
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by American Consumer Products Corp for the product Pharmacys Prescription Rubbing Alcohol (NDC 72197-030). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, when using this product, stop use, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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)
* Please review the disclaimer below.
