Isopropyl Alcohol Liquid
FDA Label NDC 24385-207

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Amerisource Bergen for the product Isopropyl Alcohol (NDC 24385-207). 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 ingredients, purpose, uses, warnings, ask a doctor before use if you have, stop use and ask a doctor if:, when using this product:, keep out of the reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Ethyl Alcohol 48%

Purpose

First Aid Antiseptic

Uses

First aid to help prevent infection in minor cuts, scrapes and burns.

Warnings

For external use only.

Ask A Doctor Before Use If You Have

deep or puncture wounds, animal bites, serious burns.

Stop Use And Ask A Doctor If:

The condition persists or gets worse, or if using this product for longer than 1 week.

When Using This Product:

Do not use in the eyes. If contact occurs, flush with large amounts of water while lifting upper and lower lids. Do not apply over large areas of the body.

Keep Out Of The Reach Of Children.

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

Directions

Clean the affected area. Aply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let it dry first.

Inactive Ingredient:

Ammoniuim Hydroxide, iodine, potasssium iodide, purified water.

Other Information:

Flammable. Keep away form fire or flame.

Store at room temperature.

* Please review the disclaimer below.