Dawn Classic

Dosage form: soap
Ingredients: Triclosan 0.1g in 100mL
Labeler: Procter & Gamble Manufacturing Company
NDC Code: 37000-613

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 Classic Lemon AB

DRUG FACTS

Active Ingredient

Triclosan 0.10%

Purpose

Antibacterial hand soap

Use
  • For handwashing to decrease bacteria on the skin

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
  • Wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

Inactive ingredients

water, sodium lauryl sulfate, sodium laureth sulfate, lauramine oxide, sodium chloride, phenoxyethanol, PEI-14 PEG-10/PPG-7 copolymer, methylisothiazolinone, fragrance, yellow 5.

Questions?

1-800-725-3296

Distributed by PROCTER & GAMBLE, CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 857 mL Bottle Label

POWERS
AWAY GREASE

CLASSIC

DAWN®

DISHWASHING LIQUID

ANTIBACTERIAL
HAND SOAP

FPO

lemon
scent

857 mL (1.81 PT)
29 FL OZ

98911136

DAWN   CLASSIC
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-613
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 
SODIUM LAURETH-3 SULFATE 
LAURAMINE OXIDE 
SODIUM CHLORIDE 
PHENOXYETHANOL 
METHYLISOTHIAZOLINONE 
FD&C YELLOW NO. 5 
Product Characteristics
ColorYELLOWScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:37000-613-15443 mL in 1 BOTTLE, PLASTIC
2NDC:37000-613-29857 mL in 1 BOTTLE, PLASTIC
3NDC:37000-613-31916 mL in 1 BOTTLE, PLASTIC
4NDC:37000-613-33975 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E02/01/201110/19/2015
Labeler - Procter & Gamble Manufacturing Company (004238200)
Establishment
NameAddressID/FEIOperations
The Procter & Gamble Manufacturing Company007130032ANALYSIS(37000-613), LABEL(37000-613), MANUFACTURE(37000-613), PACK(37000-613), RELABEL(37000-613), REPACK(37000-613)

Revised: 06/2014
 
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 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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