Carcinosin - 43742-0208-1 - (Carcinosin)

Alphabetical Index


Drug Information of Carcinosin

Product NDC: 43742-0208
Proprietary Name: Carcinosin
Non Proprietary Name: Carcinosin
Active Ingredient(s): 30    [hp_C]/mL & nbsp;   Carcinosin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Carcinosin

Product NDC: 43742-0208
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20121008

Package Information of Carcinosin

Package NDC: 43742-0208-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (43742-0208-1)

NDC Information of Carcinosin

NDC Code 43742-0208-1
Proprietary Name Carcinosin
Package Description 30 mL in 1 BOTTLE, DROPPER (43742-0208-1)
Product NDC 43742-0208
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Carcinosin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20121008
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Deseret Biologicals, Inc.
Substance Name HUMAN BREAST TUMOR CELL
Strength Number 30
Strength Unit [hp_C]/mL
Pharmaceutical Classes

Complete Information of Carcinosin


General Information