Psoriasis - 57520-0353-1 - (Arsenicum album, Borax, Graphites, Natrum muriaticum, Sepia, Sulphur,)

Alphabetical Index


Drug Information of Psoriasis

Product NDC: 57520-0353
Proprietary Name: Psoriasis
Non Proprietary Name: Arsenicum album, Borax, Graphites, Natrum muriaticum, Sepia, Sulphur,
Active Ingredient(s): 30; 30; 30; 30; 30; 30    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Arsenicum album, Borax, Graphites, Natrum muriaticum, Sepia, Sulphur,
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Psoriasis

Product NDC: 57520-0353
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20101110

Package Information of Psoriasis

Package NDC: 57520-0353-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0353-1)

NDC Information of Psoriasis

NDC Code 57520-0353-1
Proprietary Name Psoriasis
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0353-1)
Product NDC 57520-0353
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Arsenicum album, Borax, Graphites, Natrum muriaticum, Sepia, Sulphur,
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20101110
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name ARSENIC TRIOXIDE; GRAPHITE; SEPIA OFFICINALIS JUICE; SODIUM BORATE; SODIUM CHLORIDE; SULFUR
Strength Number 30; 30; 30; 30; 30; 30
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Psoriasis


General Information