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MAGNESIA PHOSPHORICA - 60512-9152-1 - (MAGNESIA PHOSPHORICA)

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Drug Information of MAGNESIA PHOSPHORICA

Product NDC: 60512-9152
Proprietary Name: MAGNESIA PHOSPHORICA
Non Proprietary Name: MAGNESIA PHOSPHORICA
Active Ingredient(s): 1    [hp_X]/1 & nbsp;   MAGNESIA PHOSPHORICA
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of MAGNESIA PHOSPHORICA

Product NDC: 60512-9152
Labeler Name: HOMEOLAB USA INC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20111130

Package Information of MAGNESIA PHOSPHORICA

Package NDC: 60512-9152-1
Package Description: 80 PELLET in 1 TUBE (60512-9152-1)

NDC Information of MAGNESIA PHOSPHORICA

NDC Code 60512-9152-1
Proprietary Name MAGNESIA PHOSPHORICA
Package Description 80 PELLET in 1 TUBE (60512-9152-1)
Product NDC 60512-9152
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MAGNESIA PHOSPHORICA
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 20111130
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name HOMEOLAB USA INC
Substance Name MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Strength Number 1
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of MAGNESIA PHOSPHORICA


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