Eczemol - 61480-127-05 - (Potassium Bromide, Nickel Sulfate, and Sulfur)

Alphabetical Index


Drug Information of Eczemol

Product NDC: 61480-127
Proprietary Name: Eczemol
Non Proprietary Name: Potassium Bromide, Nickel Sulfate, and Sulfur
Active Ingredient(s): 1; 1; 1    [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp;   Potassium Bromide, Nickel Sulfate, and Sulfur
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Eczemol

Product NDC: 61480-127
Labeler Name: Plymouth Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20011115

Package Information of Eczemol

Package NDC: 61480-127-05
Package Description: 100 TABLET in 1 BOTTLE (61480-127-05)

NDC Information of Eczemol

NDC Code 61480-127-05
Proprietary Name Eczemol
Package Description 100 TABLET in 1 BOTTLE (61480-127-05)
Product NDC 61480-127
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Bromide, Nickel Sulfate, and Sulfur
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20011115
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Plymouth Pharmaceuticals Inc
Substance Name NICKEL SULFATE; POTASSIUM BROMIDE; SULFUR
Strength Number 1; 1; 1
Strength Unit [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmaceutical Classes Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient]

Complete Information of Eczemol


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