Dawn Ultra Antibacterial Hand Apple Blossom Scent

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

Medically reviewed by Drugs.com. Last updated on Apr 15, 2024.

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

water, 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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:37000-616
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (CHLOROXYLENOL)	CHLOROXYLENOL	0.3 g in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description
1	NDC:37000-616-41	414 mL in 1 BOTTLE, PLASTIC
2	NDC:37000-616-59	591 mL in 1 BOTTLE, PLASTIC
3	NDC:37000-616-63	638 mL in 1 BOTTLE, PLASTIC
4	NDC:37000-616-70	709 mL in 1 BOTTLE, PLASTIC
5	NDC:37000-616-82	828 mL in 1 BOTTLE, PLASTIC
6	NDC:37000-616-88	887 mL in 1 BOTTLE, PLASTIC
7	NDC:37000-616-10	1010 mL in 1 BOTTLE, PLASTIC
8	NDC:37000-616-11	1120 mL in 1 BOTTLE, PLASTIC
9	NDC:37000-616-16	1660 mL in 1 BOTTLE, PLASTIC
10	NDC:37000-616-90	2660 mL in 1 BOTTLE, PLASTIC
11	NDC:37000-616-22	2210 mL in 1 BOTTLE, PLASTIC
12	NDC:37000-616-23	236 mL in 1 BOTTLE, PLASTIC
13	NDC:37000-616-43	431 mL in 1 BOTTLE, PLASTIC
14	NDC:37000-616-53	532 mL in 1 BOTTLE, PLASTIC
15	NDC:37000-616-01	2 BOTTLE, PLASTIC in 1 PACKAGE
15		638 mL in 1 BOTTLE, PLASTIC
16	NDC:37000-616-02	2 BOTTLE, PLASTIC in 1 PACKAGE
16		532 mL in 1 BOTTLE, PLASTIC
17	NDC:37000-616-03	2 BOTTLE, PLASTIC in 1 PACKAGE
17		828 mL in 1 BOTTLE, PLASTIC
18	NDC:37000-616-04	2 BOTTLE, PLASTIC in 1 PACKAGE
18		573 mL in 1 BOTTLE, PLASTIC
19	NDC:37000-616-12	1210 mL in 1 BOTTLE, PLASTIC
20	NDC:37000-616-47	479 mL in 1 BOTTLE, PLASTIC
21	NDC:37000-616-57	573 mL in 1 BOTTLE, PLASTIC
22	NDC:37000-616-20	207 mL in 1 BOTTLE, PLASTIC
23	NDC:37000-616-40	1200 mL in 1 BOTTLE, PLASTIC
24	NDC:37000-616-71	709 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/07/2014

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 04/2020

Document Id: a3f67e1e-cfc0-ae1a-e053-2995a90a9b9a

Set id: 02def70d-345d-45db-92fe-4dddd12b2194

Version: 7

Effective Time: 20200423

The Procter & Gamble Manufacturing Company

Further information

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