AMERICAN RED CROSS 50% ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid

American Red Cross 50% Isopropyl Rubbing Alcohol by

Drug Labeling and Warnings

American Red Cross 50% Isopropyl Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by MY IMPORTS USA LLC, Jell Pharmaceuticals Pvt Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl alcohol (50% conc.)

Purpose

First aid antiseptic

Uses

• first aid to help prevent the risk of infection in minor cuts, scrapes and burns 
• helps relieve minor muscular aches due to exertion

Warnings

For external use only.

Flammable,keep away from heat, spark, electrical, fire or flame

• will produce serious gastric disturbances if taken internally

Do not use

• in the eyes or apply over large areas of the body 
• longer than 1 week 
• do not inhale

Ask a doctor before use if you have

deep or punture wounds, animal bites or serious burns.

Stop use and ask a doctor if

• the condition persists or gets worse 
• irritation, pain, or redness persists or worsens
• swelling, rash, or fever develops

Kepp 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 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 

• keep tightly closed and at controlled room temperature
• does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive ingredients

purified water

Package Labeling:

INGREDIENTS AND APPEARANCE

AMERICAN RED CROSS 50% ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51628-4239
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	500 mg  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51628-4239-1	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/05/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/10/2022

Labeler - MY IMPORTS USA LLC (195767988)

Registrant - Jell Pharmaceuticals Pvt Ltd. (726025211)

Establishment
Name	Address	ID/FEI	Business Operations
Jell Pharmaceuticals Pvt Ltd.		726025211	manufacture(51628-4239)