DERMA-GLOVE- ethanol, triclosan gel

Derma-Glove by

Drug Labeling and Warnings

Derma-Glove by is a Otc medication manufactured, distributed, or labeled by RWM TECHNOLOGIES. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DESCRIPTION

DERMA-GLOVE(R) no rinse hand sanitizer gel

ACTIVE INGREDIENT

Active Ingredient

Ethanol 60%..................................................................Antimicrobial

Triclosan 0.3%..............................................................Antiseptic

PURPOSE

Antiseptic/Antimicrobial hand sanitizer gel

INDICATIONS & USAGE

• Hand sanitizer to help reduce bacteria on the skin that could cause disease
• Recommended for repeated use
  

WARNINGS AND PRECAUTIONS

Warnings

Flammable. Keep away from fire or flame.

For external use only.

When using this product do not use in or near eyes. In case of eye contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if skin irritation or redness develops and persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of the Reach of Children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions:

• Place enough product in your palm to thoroughly cover your hands
• Rub hands together briskly until dry
• Rinse with water after use
• Children under 6 years of age should be supervised when using this product
  

GENERAL PRECAUTIONS

• Do not store above 110o F (43o C)
  
• For additional information, see Material Safety Data Sheet (MSDS).

INACTIVE INGREDIENT

Deionized Water, Glycereth-18 Ethylhexanoate, Glycereth-18, Polyoxyethylene (20) Sorbitan Monooleate, 2-Amino-2-methyl-1-propanol, Acrylate crosspolymer, Polyquaternium-69, Citric Acid and Sodium Citrate

Questions or Comments?

Call 1-888-300-1225 Monday through Friday 8:00 AM to 5:00 PM

PRINCIPAL DISPLAY PANEL

LABEL

INGREDIENTS AND APPEARANCE

DERMA-GLOVE 
ethanol, triclosan gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24673-248
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ethanol (UNII: 3K9958V90M) (Ethanol - UNII:3K9958V90M)	Ethanol	0.58 g  in 1 g
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	0.03 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24673-248-01	55.2 g in 1 BOTTLE, PUMP
2	NDC: 24673-248-02	110.4 g in 1 BOTTLE, PUMP
3	NDC: 24673-248-03	220.8 g in 1 BOTTLE, PUMP
4	NDC: 24673-248-04	3532.8 g in 1 BOTTLE, PUMP
5	NDC: 24673-248-05	17664 g in 1 DRUM
6	NDC: 24673-248-06	194304 g in 1 DRUM
7	NDC: 24673-248-07	883200 g in 1 DRUM
8	NDC: 24673-248-08	1236480 g in 1 DRUM

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	02/03/2010

Labeler - RWM TECHNOLOGIES (003215779)