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Dawn Ultra Antibacterial Hand Apple Blossom Scent

Medically reviewed by Drugs.com. Last updated on Apr 23, 2020.

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

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, PPG-26, PEI-14 PEG 24/PPG-16 copolymer, sodium hydroxide, fragrance, C9-11 pareth-8, tetrasodium glutamate diacetate, yellow 5, methylisothiazolinone, 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

APPLE BLOSSOM SCENT

2X MORE* GREASE CLEANING POWER

*CLEANING INGREDIENTS PER DROP VS. NON-ULTRA DAWN

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 
ALCOHOL 
FD&C YELLOW NO. 5 
FD&C BLUE NO. 1 
WATER 
SODIUM LAURYL SULFATE 
LAURAMINE OXIDE 
SODIUM LAURETH-3 SULFATE 
PHENOXYETHANOL 
SODIUM CHLORIDE 
PPG-26 
METHYLISOTHIAZOLINONE 
SODIUM HYDROXIDE 
TETRASODIUM GLUTAMATE DIACETATE 
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
22NDC:37000-616-20207 mL in 1 BOTTLE, PLASTIC
23NDC:37000-616-401200 mL in 1 BOTTLE, PLASTIC
24NDC:37000-616-71709 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)

 
The Procter & Gamble Manufacturing Company

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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