NDC 15631-0144

COBALTUM METALLICUM

Cobaltum Metallicum

COBALTUM METALLICUM 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 Cobalt.

Product ID15631-0144_0514e002-a08c-4b46-8cb9-b54659020b68
NDC15631-0144
Product TypeHuman Otc Drug
Proprietary NameCOBALTUM METALLICUM
Generic NameCobaltum Metallicum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCOBALT
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0144-0

100 PELLET in 1 PACKAGE (15631-0144-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0144-1 [15631014401]

COBALTUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0144-0 [15631014400]

COBALTUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0144-3 [15631014403]

COBALTUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0144-4 [15631014404]

COBALTUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0144-2 [15631014402]

COBALTUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0144-5 [15631014405]

COBALTUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

Drug Details

Active Ingredients

IngredientStrength
COBALT6 [hp_X]/1

OpenFDA Data

SPL SET ID:a245b4bc-75bf-4bc7-b007-f280cd977f76
Manufacturer
UNII

NDC Crossover Matching brand name "COBALTUM METALLICUM" or generic name "Cobaltum Metallicum"

NDCBrand NameGeneric Name
0220-1442Cobaltum metallicumCOBALT
15631-0144COBALTUM METALLICUMCOBALTUM METALLICUM
37662-0441Cobaltum MetallicumCobaltum Metallicum
37662-0442Cobaltum MetallicumCobaltum Metallicum
37662-0443Cobaltum MetallicumCobaltum Metallicum
37662-0444Cobaltum MetallicumCobaltum Metallicum
37662-0445Cobaltum MetallicumCobaltum Metallicum
37662-0446Cobaltum MetallicumCobaltum Metallicum
37662-0447Cobaltum MetallicumCobaltum Metallicum
37662-0448Cobaltum MetallicumCobaltum Metallicum
68428-327Cobaltum metallicumCOBALT
71919-209Cobaltum metallicumCOBALT

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