NDC Code(s) : 24286-1529-8
Packager : DLC Laboratories, Inc.

Category : HUMAN OTC DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

De La Cruz Decolorized IodineEthyl Alcohol LIQUID
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:24286-1529
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL(UNII: 3K9958V90M)
(ALCOHOL - UNII:3K9958V90M) 		ALCOHOL0.45 mL in 1 mL
Inactive Ingredients
Ingredient Name Strength
AMMONIA(UNII: 5138Q19F1X)
IODINE(UNII: 9679TC07X4)
POTASSIUM IODIDE(UNII: 1C4QK22F9J)
WATER(UNII: 059QF0KO0R)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:24286-1529-859 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product11/06/2017
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC Monograph Drug M003 03/25/1998

LABELER - DLC Laboratories, Inc.(093351930)

REGISTRANT - Pharma Nobis, LLC(118564114)

Establishment
Name Address ID/FEI Business Operations
Pharma Nobis, LLC 118564114 manufacture(24286-1529), analysis(24286-1529), pack(24286-1529), label(24286-1529)

PRINCIPAL DISPLAY PANEL

Label