NDC Code(s) : 0395-9117-92, 0395-9117-91
Packager : Humco Holding Group, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Iodides TinctureEthyl Alcohol LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0395-9117
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:0395-9117-9259 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product30/10/2017
2NDC:0395-9117-9130 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product30/10/2017
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 03/25/1998

PRINCIPAL DISPLAY PANEL

DLC

PRINCIPAL DISPLAY PANEL

GNP

PRINCIPAL DISPLAY PANEL

Leader

PRINCIPAL DISPLAY PANEL

QC

PRINCIPAL DISPLAY PANEL

SM

PRINCIPAL DISPLAY PANEL

DDM

PRINCIPAL DISPLAY PANEL

RA

PRINCIPAL DISPLAY PANEL

CVC

PRINCIPAL DISPLAY PANEL

TC

PRINCIPAL DISPLAY PANEL

VM

PRINCIPAL DISPLAY PANEL

HM