NDC 15631-0283

MAGNESIA SULPHURICA

Magnesia Sulphurica

MAGNESIA SULPHURICA is a Oral Pellet 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 ID15631-0283_31c043f5-1d17-49b0-8342-4f585418a48b
NDC15631-0283
Product TypeHuman Otc Drug
Proprietary NameMAGNESIA SULPHURICA
Generic NameMagnesia Sulphurica
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-02
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 15631-0283-0

100 PELLET in 1 PACKAGE (15631-0283-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0283-4 [15631028304]

MAGNESIA SULPHURICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0283-3 [15631028303]

MAGNESIA SULPHURICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0283-0 [15631028300]

MAGNESIA SULPHURICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0283-1 [15631028301]

MAGNESIA SULPHURICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0283-5 [15631028305]

MAGNESIA SULPHURICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0283-2 [15631028302]

MAGNESIA SULPHURICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
MAGNESIUM SULFATE HEPTAHYDRATE1 [hp_X]/1

OpenFDA Data

SPL SET ID:0397bcf5-4708-4ec9-98cb-73dd5b6a3de7
Manufacturer
UNII

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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