DAWN ULTRA ANTIBACTERIAL HAND APPLE BLOSSOM SCENT- chloroxylenol soap

Dawn Ultra Antibacterial Hand by

Drug Labeling and Warnings

Dawn Ultra Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
C9-11 PARETH-8 (UNII: 80E6PSE1XL)
ALCOHOL (UNII: 3K9958V90M)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PPG-26 (UNII: V86KZL3H2Z)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37000-616-41	414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2014	01/10/2018
2	NDC: 37000-616-59	591 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2014	01/10/2018
3	NDC: 37000-616-63	638 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2014	12/12/2019
4	NDC: 37000-616-70	709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2014	01/10/2018
5	NDC: 37000-616-82	828 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2014
6	NDC: 37000-616-88	887 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2014	01/10/2018
7	NDC: 37000-616-10	1010 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2014	12/12/2019
8	NDC: 37000-616-11	1120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2014	01/10/2018
9	NDC: 37000-616-16	1660 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2014
10	NDC: 37000-616-90	2660 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2014	12/12/2019
11	NDC: 37000-616-22	2210 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/10/2017
12	NDC: 37000-616-23	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/10/2017	02/01/2021
13	NDC: 37000-616-43	431 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/10/2017	12/12/2019
14	NDC: 37000-616-53	532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/10/2017	12/12/2019
15	NDC: 37000-616-01	2 in 1 PACKAGE	02/10/2017	12/12/2019
15		638 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
16	NDC: 37000-616-02	2 in 1 PACKAGE	02/10/2017	12/12/2019
16		532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
17	NDC: 37000-616-03	2 in 1 PACKAGE	03/28/2018
17		828 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
18	NDC: 37000-616-04	2 in 1 PACKAGE	03/28/2018	02/01/2021
18		573 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
19	NDC: 37000-616-12	1210 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/06/2018	02/01/2021
20	NDC: 37000-616-47	479 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/06/2018
21	NDC: 37000-616-57	573 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/06/2018
22	NDC: 37000-616-20	207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/02/2019
23	NDC: 37000-616-40	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/02/2019
24	NDC: 37000-616-71	709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/02/2019

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)