50% RUBBING- isopropyl alcohol liquid

50% Rubbing by

Drug Labeling and Warnings

50% Rubbing by is a Otc medication manufactured, distributed, or labeled by TopCo Associates, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Isopropyl alcohol 50%

Purpose

First aid antiseptic

Use

helps prevent the risk of infection in:

• minor cuts
• scrapes
• 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 or puncture 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 1 week unless directed by a doctor

Stop use and ask a doctor

if condition persists or gets worse

keep out of children

If swallowed, get medical help or contact a Poison Control Center right away.

For Rubbing & Massaging

Caution - do not apply to irritated skin or if excessive irritation develops.  Avoid getting into the eyes or on mucous membranes.

Directions

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

Other Information

• does not contain, nor is intended as a substitute for grain or ethyl alcohol
• will produce serious gastric distrubances if taken internally

Inactive ingredient

water

adverse reaction

DIST. BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007

1-888-423-0139  topcare@topco.com

864.003/864AA/AC

principal display panel

TopCare

FIRST AID ANTISEPTIC

50%

Isopropyl Alcohol

For Rubbing & Massaging

• Warning Flammable Keep away from heat, spark, electrical, fire

16 FL OZ (1 PT) 473 mL

INGREDIENTS AND APPEARANCE

50% RUBBING 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 36800-864
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: 36800-864-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/03/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/03/2017

Labeler - TopCo Associates (006935977)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(36800-864)