Active Ingredients
Isopropyl Alcohol
Universal Isopropyl Rubbing Alcohol 70% - Isopropyl Alcohol Liquid
FDA Label NDC 76567-4301
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tsm Brands Llc for the product Universal Isopropyl Rubbing Alcohol 70% - Isopropyl Alcohol Liquid (NDC 76567-4301). 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, ask a doctor before use if you have, stop using this product if, keep this and all drugs out of reach of the children, purpose, when using this product, warnngs, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Ask A Doctor Before Use If You Have
Deep punctured wounds, animal bites or serious burns
Stop Using This Product If
conditions persists or gets worse
condition persist or gets worse
Keep This And All Drugs Out Of Reach Of The Children
In case of accidental ingestion, seek professional assistance or contact a Poison control control center ( 1-800-222-1222) immediately
Purpose
First aid antiseptic
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 unless directed by a doctor
Warnngs
For external use only, flammable, keep away from fire or flammable, heat, spark, electrical
Directions
clean effected area
apply small amount of this product on the area 1-3 times daily
May be covered with a sterile bandage
If bandaged, let dry firs
Inactive Ingredient
purified water
Uses
first aid to help prevent the risk of infection in minor cuts, scrapes and burns
* Please review the disclaimer below.
