Dawn Ultra Concentrated Apple Blossom

Dosage form: soap
Ingredients: Triclosan 0.1g in 100mL
Labeler: Procter & Gamble Manufacturing Company
NDC Code: 37000-605

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 Ultra Concentrated Apple Blossom 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, alcohol denat., sodium chloride, PPG-26, PEI-14 PEG-10/PPG-7 copolymer, phenoxyethanol, magnesium chloride, methylisothiazolinone, fragrance, yellow 5, blue1.

Questions?

1-800-725-3296

Distributed by PROCTER & GAMBLE, CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 1.66 L Bottle Label

DAWN HELPS
SAVE WILDLIFE
visit www.dawnsaveswildlife.com

ULTRA CONCENTRATED
DAWN®


DISHWASHING LIQUID

ANTIBACTERIAL
HAND SOAP

apple blossom®

1.66 L (1.75 QT)
56 FL OZ

99713915

FPO

DAWN   ULTRA CONCENTRATED APPLE BLOSSOM
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-605
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 
ALCOHOL 
SODIUM CHLORIDE 
PHENOXYETHANOL 
MAGNESIUM CHLORIDE 
METHYLISOTHIAZOLINONE 
FD&C YELLOW NO. 5 
FD&C BLUE NO. 1 
Product Characteristics
ColorGREENScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:37000-605-10304 mL in 1 BOTTLE, PLASTIC
2NDC:37000-605-11325 mL in 1 BOTTLE, PLASTIC
3NDC:37000-605-12375 mL in 1 BOTTLE, PLASTIC
4NDC:37000-605-14414 mL in 1 BOTTLE, PLASTIC
5NDC:37000-605-24709 mL in 1 BOTTLE, PLASTIC
6NDC:37000-605-25740 mL in 1 BOTTLE, PLASTIC
7NDC:37000-605-28828 mL in 1 BOTTLE, PLASTIC
8NDC:37000-605-29857 mL in 1 BOTTLE, PLASTIC
9NDC:37000-605-381120 mL in 1 BOTTLE, PLASTIC
10NDC:37000-605-481420 mL in 1 BOTTLE, PLASTIC
11NDC:37000-605-561660 mL in 1 BOTTLE, PLASTIC
12NDC:37000-605-902660 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(37000-605), LABEL(37000-605), MANUFACTURE(37000-605), PACK(37000-605), RELABEL(37000-605), REPACK(37000-605)

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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