ANTI-BACTERIAL GENTLE FOAMING HAND VANILLA SNAP- triclosan soap 
Bath & Body Works, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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DRUG FACTS

ACTIVE INGREDIENT

Triclosan 0.3%

PURPOSE

Antibacterial

USE

Handwashing to decrease bacteria on skin

WARNINGS

For external use only.

WHEN USING THIS PRODUCT

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

STOP USE AND ASK A DOCTOR

if irritation and redness develop.

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

  • Wet hands, work into a rich lather.
  • Rinse well.

INACTIVE INGREDIENTS

Water (Aqua, Eau), Sodium Laureth Sulfate,  Fragrance (Parfum), PPG-1-PEG-9 Lauryl Glycol Ether, Disodium Laureth Sulfosuccinate, Honey Extract (Mel, Extrait de miel),  Mangifera Indica (Mango) Fruit Extract, Olea Europaea (Olive) Fruit Extract, Cocos Nucifera (Coconut) Fruit Extract, Cocamidopropylamine Oxide, Hydroxyethyl Urea, PEG-7 Glyceryl Cocoate, Hydroxypropyl Methylcellulose, Sodium Chloride, Glycerin, Guar Hydroxypropyltrimonium Chloride, Propylene Glycol, Citric Acid, Triethylene Glycol, Tetrasodium EDTA, Benzophenone-4, Butylene Glycol,  Sodium Hydroxide, Benzyl Alcohol,  Methylchloroisothiazolinone, Methylisothiazolinone.



COMPANY INFORMATION


Bath & Body Works, Distr.
Reynoldsburg, Ohio 43068
1-800-395-1001
www.bathandbodyworks.com

PRODUCT PACKAGING

Front Label
Back Label
ANTI-BACTERIAL GENTLE FOAMING HAND  VANILLA SNAP
triclosan soap
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:62670-3898
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62670-3898-3259 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/23/201111/13/2013
Labeler - Bath & Body Works, Inc. (878952845)

Revised: 5/2011
 
Bath & Body Works, Inc.