UNIVERSAL 50% RUBBING ALCOHOL WITH WINTERGREEN AND GLYCERIN- isopropyl alcohol liquid

Universal 50% Rubbing Alcohol with Wintergreen and Glycerin by

Drug Labeling and Warnings

Universal 50% Rubbing Alcohol with Wintergreen and Glycerin 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 ingredients (by volume):

Isopropyl alcohol
(50% conc.)

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; flammable, keep away from fire or flame, heat, spark, electrical

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

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

Stop using this product if
condition persists or gets worse

Keep this and all drugs out of the reach of children.
In case of accidental ingestion, seek professional assistance or contact a Poison control center (1‑800‑222‑1222) immediately.

Directions

clean affected 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 first

Other information

store at room temperature
does not contain, nor is intended as a substitute for grain or ethyl alcohol. will produce serious gastric disturbances if taken internally.

Inactive Ingredient

purified water, wintergreen, glycerin

SPL UNCLASSIFIED SECTION

For Rubbing & Massaging

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

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

Made In Jordan

Distributed by: Universal Distribution Center
96 Distribution Boulevard Edison, NJ 08817

Packaging

INGREDIENTS AND APPEARANCE

UNIVERSAL 50% RUBBING ALCOHOL WITH WINTERGREEN AND GLYCERIN 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-412
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	50 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
METHYL SALICYLATE (UNII: LAV5U5022Y)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-412-32	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/01/2023

Labeler - Universal Distribution Center LLC (019180459)