NDC 15631-0281

MAGNESIA MURIATICA

Magnesia Muriatica

MAGNESIA MURIATICA 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 Chloride.

Product ID15631-0281_63f0c164-1c0e-4144-8248-52ec8b834c29
NDC15631-0281
Product TypeHuman Otc Drug
Proprietary NameMAGNESIA MURIATICA
Generic NameMagnesia Muriatica
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-09
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameMAGNESIUM CHLORIDE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0281-0

100 PELLET in 1 PACKAGE (15631-0281-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0281-2 [15631028102]

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

NDC 15631-0281-0 [15631028100]

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

NDC 15631-0281-4 [15631028104]

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

NDC 15631-0281-3 [15631028103]

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

NDC 15631-0281-1 [15631028101]

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

NDC 15631-0281-5 [15631028105]

MAGNESIA MURIATICA 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 CHLORIDE1 [hp_X]/1

OpenFDA Data

SPL SET ID:0e92fd6c-7696-4a33-9713-0daab5ce5a55
Manufacturer
UNII

NDC Crossover Matching brand name "MAGNESIA MURIATICA" or generic name "Magnesia Muriatica"

NDCBrand NameGeneric Name
0220-3254Magnesia muriaticaMAGNESIUM CHLORIDE
0220-3256Magnesia muriaticaMAGNESIUM CHLORIDE
0220-3259Magnesia muriaticaMAGNESIUM CHLORIDE
0220-3260Magnesia muriaticaMAGNESIUM CHLORIDE
10191-1973MAGNESIA MURIATICAMAGNESIUM CHLORIDE
15631-0281MAGNESIA MURIATICAMAGNESIA MURIATICA
37662-1021Magnesia MuriaticaMagnesia Muriatica
37662-1022Magnesia MuriaticaMagnesia Muriatica
37662-1023Magnesia MuriaticaMagnesia Muriatica
37662-1024Magnesia MuriaticaMagnesia Muriatica
37662-1025Magnesia MuriaticaMagnesia Muriatica
37662-1026Magnesia MuriaticaMagnesia Muriatica
37662-1027Magnesia MuriaticaMagnesia Muriatica
37662-1028Magnesia MuriaticaMagnesia Muriatica
68428-488Magnesia muriaticaMAGNESIUM CHLORIDE
71919-434Magnesia muriaticaMAGNESIUM CHLORIDE
61495-101Cramp-ZMagnesia Muriatica
61495-401Fibro FlexMagnesia Muriatica

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