UNIVERSAL RUBBING ALCOHOL- isopropyl alcohol liquid

Universal Rubbing Alcohol by

Drug Labeling and Warnings

Universal Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient:

Isopropyl alcohol 91%

Purpose

First Aid Antiseptic

Uses

first aid to help prevent the risk of infection in minor cuts, scrapes and burns.

Warnings

For external use only.

 if taken internally, serious gastric disturbances will occur
flammable, keep away from fire or flame, heat, spark, electrical
use only in a well-ventilated area; fumes may be toxic

Ask a doctor before use if you have deep puncture wounds, animal bites, or serious burns

When using this product  do not get into eyes  do not inhale do not apply over large areas of the body do not use longer than one week unless directed by a doctor

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 (1‑800‑222‑1222) right away.

Directions

clean the affected area apply small amount of product on the affected area 1 to 3 times a day may be covered with a sterile bandage If bandaged, let dry first

Other information

store at controlled room temperature does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive Ingredient

Purified Water

SPL UNCLASSIFIED SECTION

For Rubbing & Massaging

Use only in a well-ventilated area. Fumes may be harmful.

TAMPER EVIDENT: DO NOT USE IF THE PRINTED SAFETY FOIL UNDER THE CAP IS BROKEN OR MISSING.

Made in Turkey

Mfd for and Distributed By:
Universal Distribution Center LLC
330 Applegarth Road, Monroe Township, NJ 08831
www.universaldc.com

Packaging

INGREDIENTS AND APPEARANCE

UNIVERSAL RUBBING ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-406
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	91 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-406-35	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2023
2	NDC: 52000-406-36	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/01/2023

Labeler - Universal Distribution Center LLC (019180459)