DT ANTIBACTERIAL FOAMING HAND WASH- triclosan liquid

DT Antibacterial Foaming Hand Wash by

Drug Labeling and Warnings

DT Antibacterial Foaming Hand Wash by is a Otc medication manufactured, distributed, or labeled by Volume Distributors, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Triclosan 0.15%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses:

for hand washing to decrease bacteria on the skin.

WARNINGS

Warnings for external use only.

WHEN USING

When using this product avoid contact with eyes. In case of eye contact, flush with water.

STOP USE

Stop use and ask a doctor if irritation and redness develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

pump into hands

lather vigorously for at least 15 seconds

rinse and dry thoroughly.

INACTIVE INGREDIENT

Inactive Ingredients

Water (aqua), sodium laureth sulfate, cocamide DEA, cocamidopropyl betaine, glycerin, citric acid, kathom CG, Fragrance, FD and C yellow No.5, FDandC Red No 40.

PRINCIPAL DISPLAY PANEL

DT for your Daily Touch
Antibacterial
foaming Hand Wash

Distributed by DT Products
Vernon, CA 90058
MADE IN CHINA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DT ANTIBACTERIAL FOAMING HAND WASH 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50523-632
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.15 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50523-632-08	221 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/22/2010

Labeler - Volume Distributors, Inc. (002029544)