NDC 15631-0350

PLATINUM MURIATICUM

Platinum Muriaticum

PLATINUM 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 Platinic Chloride Hexahydrate.

Product ID15631-0350_33eb018b-1b83-4732-9199-6246d49b6e65
NDC15631-0350
Product TypeHuman Otc Drug
Proprietary NamePLATINUM MURIATICUM
Generic NamePlatinum Muriaticum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NamePLATINIC CHLORIDE HEXAHYDRATE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0350-0

100 PELLET in 1 PACKAGE (15631-0350-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0350-5 [15631035005]

PLATINUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0350-4 [15631035004]

PLATINUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0350-3 [15631035003]

PLATINUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0350-0 [15631035000]

PLATINUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0350-2 [15631035002]

PLATINUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0350-1 [15631035001]

PLATINUM MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

Drug Details

Active Ingredients

IngredientStrength
PLATINIC CHLORIDE HEXAHYDRATE3 [hp_X]/1

OpenFDA Data

SPL SET ID:636974ec-63b5-4216-bb07-b8110fb9ab0f
Manufacturer
UNII

NDC Crossover Matching brand name "PLATINUM MURIATICUM" or generic name "Platinum Muriaticum"

NDCBrand NameGeneric Name
15631-0350PLATINUM MURIATICUMPLATINUM MURIATICUM
71919-546Platinum muriaticumPLATINIC CHLORIDE HEXAHYDRATE

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