UNIVERSAL ISOPROPYL RUBBING ALCOHOL 70% - ISOPROPYL ALCOHOL LIQUID liquid

UNIVERSAL ISOPROPYL RUBBING ALCOHOL 70% - isopropyl alcohol liquid by

Drug Labeling and Warnings

UNIVERSAL ISOPROPYL RUBBING ALCOHOL 70% - isopropyl alcohol liquid by is a Otc medication manufactured, distributed, or labeled by TSM BRANDS LLC, TSM BRANDS KIMYA SANAYI VE DIS TICARET ANONIM SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Isopropyl Alcohol

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

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

Stop using this product if

condition persist or gets worse

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

Label

INGREDIENTS AND APPEARANCE

UNIVERSAL ISOPROPYL RUBBING ALCOHOL 70% - ISOPROPYL ALCOHOL LIQUID 
universal isopropyl rubbing alcohol 70% - isopropyl alcohol liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76567-4301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	331 mL  in 473 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	142 mL  in 473 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76567-4301-6	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/17/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/17/2025

Labeler - TSM BRANDS LLC (079777521)

Establishment
Name	Address	ID/FEI	Business Operations
TSM BRANDS KIMYA SANAYI VE DIS TICARET ANONIM SIRKETI		533120570	manufacture(76567-4301)