NDC Code 37000-617-10 | pharmacompass.com

NDC Code(s) : 37000-617-26, 37000-617-59, 37000-617-63, 37000-617-70, 37000-617-10, 37000-617-11, 37000-617-16, 37000-617-23, 37000-617-53, 37000-617-22, 37000-617-47, 37000-617-57, 37000-617-12, 37000-617-82, 37000-617-20, 37000-617-40, 37000-617-19, 37000-617-38, 37000-617-21, 37000-617-54, 37000-617-65
Packager : The Procter & Gamble Manufacturing Company

Category : HUMAN OTC DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Dawn Ultra Antibacterial Hand Chloroxylenol SOAP

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:37000-617
Route of Administration	TOPICAL	DEA Schedule

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

Ingredient Name	Strength
Inactive Ingredients
TETRASODIUM GLUTAMATE DIACETATE(UNII: 5EHL50I4MY)
DECETH-8(UNII: 19FQ96EA8Q)
ALCOHOL(UNII: 3K9958V90M)
WATER(UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
LAURAMINE OXIDE(UNII: 4F6FC4MI8W)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
SODIUM CHLORIDE(UNII: 451W47IQ8X)
PPG-26(UNII: V86KZL3H2Z)
FD&C YELLOW NO. 5(UNII: I753WB2F1M)
D&C RED NO. 33(UNII: 9DBA0SBB0L)
SODIUM HYDROXIDE(UNII: 55X04QC32I)
C9-11 PARETH-8(UNII: 80E6PSE1XL)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:37000-617-26	266 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	07/07/2014
2	NDC:37000-617-59	591 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	07/07/2014
3	NDC:37000-617-63	638 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	07/07/2014
4	NDC:37000-617-70	709 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	07/07/2014
5	NDC:37000-617-10	1010 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	07/07/2014
6	NDC:37000-617-11	1120 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	07/07/2014
7	NDC:37000-617-16	1660 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	07/07/2014
8	NDC:37000-617-23	236 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	02/10/2017
9	NDC:37000-617-53	532 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	02/10/2017
10	NDC:37000-617-22	2210 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	02/10/2017
11	NDC:37000-617-47	479 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	02/02/2018
12	NDC:37000-617-57	573 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	02/02/2018
13	NDC:37000-617-12	1210 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	02/02/2018
14	NDC:37000-617-82	828 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	02/02/2018
15	NDC:37000-617-20	207 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	04/02/2019
16	NDC:37000-617-40	1200 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	04/02/2019
17	NDC:37000-617-19	192 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	30/12/2021
18	NDC:37000-617-38	1120 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	30/12/2021
19	NDC:37000-617-21	221 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	12/01/2022
20	NDC:37000-617-54	532 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	02/07/2023
21	NDC:37000-617-65	650 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product	02/07/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M003	07/07/2014

LABELER - The Procter & Gamble Manufacturing Company(004238200)

NDC 37000-617-10
API & Excipient Details

marketed by The Procter & Gamble Manufacturing Company under NDC Code 37000-617-10

INGREDIENTS AND APPEARANCE

PRINCIPAL DISPLAY PANEL

NDC 37000-617-10 API & Excipient Details

marketed by The Procter & Gamble Manufacturing Company under NDC Code 37000-617-10

INGREDIENTS AND APPEARANCE

PRINCIPAL DISPLAY PANEL

NDC 37000-617-10
API & Excipient Details