DT ANTIBACTERIAL HAND

Dosage form: soap
Ingredients: TRICLOSAN .015mL in 100mL
Labeler: VOLUME DISTRIBUTORS
NDC Code: 50523-567

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.

DT ANTIBACTERIAL HAND SOAP

Anibacterial Hand soap with moisturizer

ACTIVE INGREDIENT                                    PURPOSE

 Triclosan 0.15%                                             Antibacterial


PURPOSE
Antibacterial

USES

For handwashing to decrease bacteria on the skin.

WARNINGS

For external use only


When using this product, avoid contact with eyes.

In case of eye contact, flush with water.

Stop use and ask a doctor if irritation and redness develops

Keep out of reach of children.

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

Directions

Pump into hands, wet as needed. Lather vigorously for at least 15 seconds. Wash skin, rinse and dry thoroughly.

Water, sodium laureth sulfate, ammonium lauryl sulfate, decyl glucoside, cocamidopropyl betaine, glycerin, sodium chloride, PEG-18 glyceryl oleate/cocoate, fragrance, cocamide MEA, DMDM Hydantoin, tetrasodium EDTA, citric acid, FDandC yellow 5, FDandC red4

DISTRIBUTED BY:

DT PRODUCTS

VERNON, CA 90058

MADE IN CHINA

DT

FOR YOUR DAILY TOUCH

SPECIAL VALUE

Antibacterial

Hand Soap

WITH MOISTURIZERS

LEAVE HANDS FEELING SOFT AND REFRESHED.

16.9 FL OZ (500 ML)

DT ANTIBACTERIAL HAND 
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50523-567
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN.015 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH SULFATE 
AMMONIUM LAURYL SULFATE 
COCAMIDOPROPYL BETAINE 
GLYCERIN 
SODIUM CHLORIDE 
DMDM HYDANTOIN 
EDETATE SODIUM 
CITRIC ACID MONOHYDRATE 
Packaging
#Item CodePackage Description
1NDC:50523-567-16500 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/15/2010
Labeler - VOLUME DISTRIBUTORS (002029544)

Revised: 12/2010
 
VOLUME DISTRIBUTORS

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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