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Dawn Direct Foam Citrus Kick

Dosage form: soap
Ingredients: Triclosan 0.1g in 100mL
Labeler: Procter & Gamble Manufacturing Company
NDC Code: 37000-610

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.

Dawn Direct Foam Citrus Kick AB

DRUG FACTS

Active Ingredient

Triclosan 0.10%

Purpose

Antibacterial hand soap

Use
  • helps fight germs on hands when used as a hand soap

Warnings

For external use only

Keep out of reach of children

In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

Directions
  • Wash hands and rinse

Inactive ingredients

water, sodium lauryl sulfate, phenoxyisopropanol, SD alcohol, sodium laureth sulfate, C12-14-16, dimethyl amine oxide, glycerol, sodium cumenesulfonate, propylene glycol, sodium chloride, terpineol, cyclohexanediamine, phenoxyethanol, fragrance

Questions?

1-800-725-3296

Distr. by PROCTER & GAMBLE, CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 300 mL Bottle Label

DAWN®
Ⓤ

190
PUMPS

DIRECT FOAM™

ANTIBACTERIAL
HAND SOAP

Citrus Kick
DISHWASHING FOAM

300 mL 10.1 FL OZ

99299586

FPO

DAWN   DIRECT FOAM CITRUS KICK
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-610
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Triclosan (Triclosan) Triclosan0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURYL SULFATE 
PHENOXYISOPROPANOL 
ALCOHOL 
SODIUM LAURETH SULFATE 
LAURAMINE OXIDE 
GLYCERIN 
SODIUM CUMENESULFONATE 
PROPYLENE GLYCOL 
SODIUM CHLORIDE 
TERPINEOL 
PHENOXYETHANOL 
Packaging
#Item CodePackage Description
1NDC:37000-610-10300 mL in 1 BOTTLE, PUMP
2NDC:37000-610-13400 mL in 1 BOTTLE, PUMP
3NDC:37000-610-30915 mL in 1 BOTTLE, PUMP
4NDC:37000-610-31928 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E12/01/2008
Labeler - Procter & Gamble Manufacturing Company (004238200)
Establishment
NameAddressID/FEIOperations
The Procter & Gamble Manufacturing Company007130032ANALYSIS, LABEL, MANUFACTURE, PACK, RELABEL, REPACK

Revised: 10/2011
Document Id: 2eb2ff5c-05d1-49ec-b2bf-8e887916a329
Set id: df66e44d-7242-4669-9ea3-8f572fce89e0
Version: 1
Effective Time: 20111025
 
Procter & Gamble Manufacturing Company

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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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