NDC Code(s) : 65517-1015-1
Packager : Dukal Corporation

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

DawnMist Antiperspirant Deodorant ALUMINUM CHLOROHYDRATE GEL
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65517-1015
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALUMINUM CHLOROHYDRATE(UNII: HPN8MZW13M)
(ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) 		ALUMINUM CHLOROHYDRATE150 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
HYPROMELLOSES(UNII: 3NXW29V3WO)
PEG-12 DIMETHICONE (300 CST)(UNII: ZEL54N6W95)
PEG-40 CASTOR OIL(UNII: 4ERD2076EF)
DIAZOLIDINYL UREA(UNII: H5RIZ3MPW4)
IODOPROPYNYL BUTYLCARBAMATE(UNII: 603P14DHEB)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:65517-1015-13 mL in 1 PACKET
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part350 05/02/2013

PRINCIPAL DISPLAY PANEL

DeodorantLabel