BEBELLE FOR KIDS ANTIBACTERIAL HAND- triclosan soap

Bebelle for Kids Antibacterial Hand by

Drug Labeling and Warnings

Bebelle for Kids Antibacterial Hand 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 0.2%

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), ammonium lauryl sulfate, ammonium chloride, lauramide DEA, DMDM hydantoin, fragrance, citric acid, tatrasodium EDTA, FD and C Red No. 40

PRINCIPAL DISPLAY PANEL

Bebelle

For Kids

Gently cleanses and kills germs

Antibacterial Hand Soap

Strawberry

Distributed by

Bebelle Products

Vernon, CA 90058

MADE IN CHINA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BEBELLE FOR KIDS ANTIBACTERIAL HAND 
triclosan soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50523-546
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)
DMDM HYDANTOIN (UNII: BYR0546TOW)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50523-546-75	221 mL in 1 BOTTLE; Type 0: Not a Combination Product

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)