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Apis compositum - 50114-6010-2 - (TURPENTINE OIL and NUTMEG and APIS MELLIFERA and STRYCHNOS IGNATII SEED and VERATRUM ALBUM ROOT and PHOSPHORUS and MERCURIC CHLORIDE)

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Drug Information of Apis compositum

Product NDC: 50114-6010
Proprietary Name: Apis compositum
Non Proprietary Name: TURPENTINE OIL and NUTMEG and APIS MELLIFERA and STRYCHNOS IGNATII SEED and VERATRUM ALBUM ROOT and PHOSPHORUS and MERCURIC CHLORIDE
Active Ingredient(s): 4; 8; 6; 6; 4; 6; 4    [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg & nbsp;   TURPENTINE OIL and NUTMEG and APIS MELLIFERA and STRYCHNOS IGNATII SEED and VERATRUM ALBUM ROOT and PHOSPHORUS and MERCURIC CHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Apis compositum

Product NDC: 50114-6010
Labeler Name: Heel Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19840131

Package Information of Apis compositum

Package NDC: 50114-6010-2
Package Description: 30000 mg in 1 BOTTLE (50114-6010-2)

NDC Information of Apis compositum

NDC Code 50114-6010-2
Proprietary Name Apis compositum
Package Description 30000 mg in 1 BOTTLE (50114-6010-2)
Product NDC 50114-6010
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TURPENTINE OIL and NUTMEG and APIS MELLIFERA and STRYCHNOS IGNATII SEED and VERATRUM ALBUM ROOT and PHOSPHORUS and MERCURIC CHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19840131
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Heel Inc.
Substance Name APIS MELLIFERA; MERCURIC CHLORIDE; NUTMEG; PHOSPHORUS; STRYCHNOS IGNATII SEED; TURPENTINE OIL; VERATRUM ALBUM ROOT
Strength Number 4; 8; 6; 6; 4; 6; 4
Strength Unit [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg
Pharmaceutical Classes

Complete Information of Apis compositum


General Information