ECZEMA - 60512-6009-0 - (FUMARIA OFFICINALIS, NATRUM MURIATICUM, AGARICUS MUSCARIUS, PETROLEUM, SEPIA, KALI ARSENICOSUM, ALUMINA)

Alphabetical Index


Drug Information of ECZEMA

Product NDC: 60512-6009
Proprietary Name: ECZEMA
Non Proprietary Name: FUMARIA OFFICINALIS, NATRUM MURIATICUM, AGARICUS MUSCARIUS, PETROLEUM, SEPIA, KALI ARSENICOSUM, ALUMINA
Active Ingredient(s): 6; 6; 6; 6; 6; 6; 6    [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 & nbsp;   FUMARIA OFFICINALIS, NATRUM MURIATICUM, AGARICUS MUSCARIUS, PETROLEUM, SEPIA, KALI ARSENICOSUM, ALUMINA
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of ECZEMA

Product NDC: 60512-6009
Labeler Name: HOMEOLAB USA INC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20120725

Package Information of ECZEMA

Package NDC: 60512-6009-0
Package Description: 90 TABLET, CHEWABLE in 1 BOTTLE (60512-6009-0)

NDC Information of ECZEMA

NDC Code 60512-6009-0
Proprietary Name ECZEMA
Package Description 90 TABLET, CHEWABLE in 1 BOTTLE (60512-6009-0)
Product NDC 60512-6009
Product Type Name HUMAN OTC DRUG
Non Proprietary Name FUMARIA OFFICINALIS, NATRUM MURIATICUM, AGARICUS MUSCARIUS, PETROLEUM, SEPIA, KALI ARSENICOSUM, ALUMINA
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20120725
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name HOMEOLAB USA INC.
Substance Name ALUMINUM OXIDE; AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY; FUMARIA OFFICINALIS FLOWERING TOP; KEROSENE; POTASSIUM ARSENITE ANHYDROUS; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE
Strength Number 6; 6; 6; 6; 6; 6; 6
Strength Unit [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
Pharmaceutical Classes

Complete Information of ECZEMA


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