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Dawn Ultra Antibacterial Hand Apple Blossom Scent

Medically reviewed on December 13, 2017.

Dosage form: soap
Ingredients: CHLOROXYLENOL 0.3g in 100mL
Labeler: The Procter & Gamble Manufacturing Company
NDC Code: 37000-616

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 Antibacterial Hand

Apple Blossom ® Scent

Drug Facts

Active ingredient

Chloroxylenol 0.30%

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

‚Äčwater, sodium lauryl sulfate, lauramine oxide, sodium laureth sulfate, alcohol denat., phenoxyethanol, sodium chloride, C9-11 pareth-8, chloroxylenol, PPG-26, sodium hydroxide, PEI-14 PEG-24/PPG-16 copolymer, fragrance, tetrasodium dicarboxymethyl glutamate, methylisothiazolinone, yellow 5, blue 1.

Questions?

1-800-725-3296

Distributed by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 1.66 L Bottle Label

DAWN ®
ULTRA

ANTIBACTERIAL
HAND SOAP

2X MORE* GREASE CLEANING POWER

*CLEANING INGREDIENTS PER DROP VS. NON-ULTRA DAWN

apple blossom ® scent
DISHWASHING LIQUID

1.66 L (1.75 QT) 56 FL OZ

DAWN ULTRA ANTIBACTERIAL HAND  APPLE BLOSSOM SCENT
chloroxylenol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-616
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
C9-11 PARETH-8 
SODIUM HYDROXIDE 
FD&C YELLOW NO. 5 
FD&C BLUE NO. 1 
ALCOHOL 
WATER 
SODIUM LAURYL SULFATE 
LAURAMINE OXIDE 
SODIUM LAURETH-3 SULFATE 
PHENOXYETHANOL 
SODIUM CHLORIDE 
PPG-26 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:37000-616-41414 mL in 1 BOTTLE, PLASTIC
2NDC:37000-616-59591 mL in 1 BOTTLE, PLASTIC
3NDC:37000-616-63638 mL in 1 BOTTLE, PLASTIC
4NDC:37000-616-70709 mL in 1 BOTTLE, PLASTIC
5NDC:37000-616-82828 mL in 1 BOTTLE, PLASTIC
6NDC:37000-616-88887 mL in 1 BOTTLE, PLASTIC
7NDC:37000-616-101010 mL in 1 BOTTLE, PLASTIC
8NDC:37000-616-111120 mL in 1 BOTTLE, PLASTIC
9NDC:37000-616-161660 mL in 1 BOTTLE, PLASTIC
10NDC:37000-616-902660 mL in 1 BOTTLE, PLASTIC
11NDC:37000-616-222210 mL in 1 BOTTLE, PLASTIC
12NDC:37000-616-23236 mL in 1 BOTTLE, PLASTIC
13NDC:37000-616-43431 mL in 1 BOTTLE, PLASTIC
14NDC:37000-616-53532 mL in 1 BOTTLE, PLASTIC
15NDC:37000-616-012 BOTTLE, PLASTIC in 1 PACKAGE
15638 mL in 1 BOTTLE, PLASTIC
16NDC:37000-616-022 BOTTLE, PLASTIC in 1 PACKAGE
16532 mL in 1 BOTTLE, PLASTIC
17NDC:37000-616-032 BOTTLE, PLASTIC in 1 PACKAGE
17828 mL in 1 BOTTLE, PLASTIC
18NDC:37000-616-042 BOTTLE, PLASTIC in 1 PACKAGE
18573 mL in 1 BOTTLE, PLASTIC
19NDC:37000-616-121210 mL in 1 BOTTLE, PLASTIC
20NDC:37000-616-47479 mL in 1 BOTTLE, PLASTIC
21NDC:37000-616-57573 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/07/2014
Labeler - The Procter & Gamble Manufacturing Company (004238200)
Establishment
NameAddressID/FEIOperations
The Procter & Gamble Manufacturing Company007130032manufacture(37000-616), pack(37000-616)

 
The 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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