RUBBING- ethyl alcohol liquid

Rubbing by

Drug Labeling and Warnings

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

Ethyl alcohol 70%

Purpose

First aid antiseptic

Use

first aid to help 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 the eyes or on mucous membranes.  Avoid inhaling this product.

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 bandage, let dry first

other information

will produce serious gastric disturbances if taken internally

Inactive ingredient

acetone, denatonium benzoate, methyl isobutyl ketone, water

SPL UNCLASSIFIED SECTION

Distributed by: Geiss, Destin & Dunn, Inc

Peachtree City, GA 30269

www.valuelabels.com

876.002/876AC

principal display panel

NDC: 50804-876-43

Good Sense

Ethyl Rubbing Alcohol

70% by volume

• First Aid Antiseptic
• For Rubbing and Massaging

WARNING FLAMMABLE Keep awa from heat, spark, electrical, fire or flame

Use only in a well ventilated area: fumes can be harmful

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

16 FL OZ (1 PT) 473 mL

INGREDIENTS AND APPEARANCE

RUBBING 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50804-876
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	610 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACETONE (UNII: 1364PS73AF)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
METHYL ISOBUTYL KETONE (UNII: U5T7B88CNP)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50804-876-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/18/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/18/2009

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

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(50804-876)