50% RUBBING- isopropyl alcohol liquid

50% Rubbing by

Drug Labeling and Warnings

50% Rubbing by is a Otc medication manufactured, distributed, or labeled by Greenbrier International, Inc., Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Isopropyl alcohol 50%

Purpose

First aid antiseptic

Uses

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

for deep or 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 1 week

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 right away.

Caution

Fumes can be acutely irritating to skin, eyes and the respiratory system.  Do not apply to irritated skin or if excessive irritation develops.  Avoid getting into eyes or on mucous membranes.  Avoid inhaling this product.

Directions

• clean the affected area
• apply a small amount of the is 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

Inactive ingredient

water

adverse reaction

Distributed By Greenbrier International, Inc.

500 Volvo Parkway, Chesapeake, VA 23320

Pat. D675,101

864.003/864AA-AC

Principal Display Panel

ASSURED

FIRST AID ANTISEPTIC

50% ISOPROPYL

Rubbing

Alcohol

WARNING FLAMMABLE - Keep away from heat, spart, electrical, fire or flame

Use only in a well-ventilated area; fumes can be harmful

CAUTION: Do not point at self or others; product wil squirt when squeezed.

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: 33992-0864
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: 33992-0864-3	177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/08/2014
2	NDC: 33992-0864-1	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/08/2014
3	NDC: 33992-0864-4	710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/08/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/08/2014

Labeler - Greenbrier International, Inc. (610322518)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(33992-0864)