50% RUBBING- isopropyl alcohol liquid

50% Rubbing by

Drug Labeling and Warnings

50% Rubbing by is a Otc medication manufactured, distributed, or labeled by Geiss, Destin & Dunn, Inc, Vi-Jon. 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
• scarapes
• 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 reach of children.

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

Caution

For Rubbing & Massage: Caution-Do not apply to irritated skind or if excessive irritation develops.  Avoid getting into the eyes or on mucous membranes

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
• will produce serious gastric distrubances if taken internally

Inactive ingredient

water

Adverse Reactions

Distributed by Geiss, Destin & Dunn, Inc

Peachtree City, Ga 30269

www.valuelabels.com

864.003/864AC

principal display panel

NDC 50804-864-43

GOODSENSE

50%

Isopopyl

Alcohol

• First Aid Antiseptic
• For Rubbing and Massaging

100%

SATISFACTION

GUARANTED

Square bottle uses less platic than a siilarly sized round bottle

Recyclable (If available in your area)WARNING FLAMMABLE - Keep away from hear, spark, electrical, fire or flame

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: 50804-864
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: 50804-864-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/21/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/21/2010

Labeler - Geiss, Destin & Dunn, Inc (076059836)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(50804-864)