NDC 15631-0191

FERRUM MURIATICUM

Ferrum Muriaticum

FERRUM MURIATICUM 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 Ferric Chloride Hexahydrate.

Product ID15631-0191_35423751-167e-4761-9c6c-44ff30f98ccc
NDC15631-0191
Product TypeHuman Otc Drug
Proprietary NameFERRUM MURIATICUM
Generic NameFerrum Muriaticum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-25
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameFERRIC CHLORIDE HEXAHYDRATE
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0191-0

100 PELLET in 1 PACKAGE (15631-0191-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0191-0 [15631019100]

FERRUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0191-3 [15631019103]

FERRUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0191-1 [15631019101]

FERRUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0191-5 [15631019105]

FERRUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0191-2 [15631019102]

FERRUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0191-4 [15631019104]

FERRUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
FERRIC CHLORIDE HEXAHYDRATE2 [hp_X]/1

OpenFDA Data

SPL SET ID:2c17bf80-5791-4f2e-8536-8ab56575cbb1
Manufacturer
UNII

NDC Crossover Matching brand name "FERRUM MURIATICUM" or generic name "Ferrum Muriaticum"

NDCBrand NameGeneric Name
15631-0191FERRUM MURIATICUMFERRUM MURIATICUM
37662-0718Ferrum MuriaticumFerrum Muriaticum
37662-0719Ferrum MuriaticumFerrum Muriaticum
37662-0720Ferrum MuriaticumFerrum Muriaticum
37662-0721Ferrum MuriaticumFerrum Muriaticum
37662-0722Ferrum MuriaticumFerrum Muriaticum
37662-0723Ferrum MuriaticumFerrum Muriaticum
37662-0724Ferrum MuriaticumFerrum Muriaticum
53645-1910Ferrum MuriaticumFerrum Muriaticum
68428-384Ferrum muriaticumFERRIC CHLORIDE HEXAHYDRATE
71919-290Ferrum muriaticumFERRIC CHLORIDE HEXAHYDRATE

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