Isopropyl Alcohol Liquid
FDA Label NDC 53329-800

14 label sections · Submitted to the FDA by Medline Industries, Lp · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Medline Industries, Lp for the product Isopropyl Alcohol (NDC 53329-800). 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, do not use, when using this product do not, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Isopropyl Alcohol 70%

Purpose

First Aid Antiseptic

Uses

For first aid to help prevent the risk of infection in minor:

  • cuts
  • scrapes
  • burns

Warnings

For external use only.

Flammable. Keep away from fire or flame, heat, spark, electrical

Do Not Use

with electrocautery procedures. Use only in a well ventilated area; fumes may be harmful

When Using This Product Do Not

  • get into eyes
  • inhale
  • apply over large areas of the body.
  • use longer than 1 week

Stop Use And Ask A Doctor If

condition persists or gets worse

Keep Out Of Reach Of Children.

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

Directions

  • Clean the affected area. Apply a small amount of the product on the area 1 to 3 times daily.
  • May be covered with a sterile bandage.
  • If bandaged, let dry first.

Other Information

  • Does not contain, nor is intended as a substitute for grain or ethyl alcohol.
  • Will produce serious gastric disturbances if taken internally

Inactive Ingredients

Water

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