NDC 15631-0631

MAGNESIA SULPHURICA

Magnesia Sulphurica

MAGNESIA SULPHURICA is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Magnesium Sulfate Heptahydrate.

Product ID15631-0631_2a322647-663f-4204-b312-9a77f1f9d8c3
NDC15631-0631
Product TypeHuman Otc Drug
Proprietary NameMAGNESIA SULPHURICA
Generic NameMagnesia Sulphurica
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-26
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameMAGNESIUM SULFATE HEPTAHYDRATE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0631-0

1 TABLET in 1 BLISTER PACK (15631-0631-0)
Marketing Start Date2015-12-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0631-5 [15631063105]

MAGNESIA SULPHURICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0631-0 [15631063100]

MAGNESIA SULPHURICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0631-3 [15631063103]

MAGNESIA SULPHURICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0631-4 [15631063104]

MAGNESIA SULPHURICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0631-6 [15631063106]

MAGNESIA SULPHURICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0631-7 [15631063107]

MAGNESIA SULPHURICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0631-1 [15631063101]

MAGNESIA SULPHURICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0631-2 [15631063102]

MAGNESIA SULPHURICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
MAGNESIUM SULFATE HEPTAHYDRATE1 [hp_X]/1

OpenFDA Data

SPL SET ID:14a3696b-9a88-4ea5-8357-d98356c14d7b
Manufacturer
UNII
UPC Code
  • 8907460005526

    • NDC Crossover Matching brand name "MAGNESIA SULPHURICA" or generic name "Magnesia Sulphurica"

    NDCBrand NameGeneric Name
    0220-3267Magnesia sulphuricaMAGNESIUM SULFATE HEPTAHYDRATE
    15631-0283MAGNESIA SULPHURICAMAGNESIA SULPHURICA
    15631-0631MAGNESIA SULPHURICAMAGNESIA SULPHURICA
    37662-1029Magnesia SulphuricaMagnesia Sulphurica
    37662-1030Magnesia SulphuricaMagnesia Sulphurica
    37662-1031Magnesia SulphuricaMagnesia Sulphurica
    37662-1032Magnesia SulphuricaMagnesia Sulphurica
    37662-1033Magnesia SulphuricaMagnesia Sulphurica
    37662-1034Magnesia SulphuricaMagnesia Sulphurica
    37662-1035Magnesia SulphuricaMagnesia Sulphurica
    37662-1036Magnesia SulphuricaMagnesia Sulphurica
    68428-980Magnesia sulphuricaMAGNESIUM SULFATE HEPTAHYDRATE
    71919-437Magnesia sulphuricaMAGNESIUM SULFATE HEPTAHYDRATE
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