NDC 15631-0081

BISMUTHUM METALLICUM

Bismuthum Metallicum

BISMUTHUM 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 Bismuth.

Product ID15631-0081_9ed9a8ea-8752-b0d7-e053-2a95a90acf04
NDC15631-0081
Product TypeHuman Otc Drug
Proprietary NameBISMUTHUM METALLICUM
Generic NameBismuthum Metallicum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameBISMUTH
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0081-0

100 PELLET in 1 PACKAGE (15631-0081-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0081-5 [15631008105]

BISMUTHUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0081-3 [15631008103]

BISMUTHUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0081-0 [15631008100]

BISMUTHUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0081-1 [15631008101]

BISMUTHUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0081-4 [15631008104]

BISMUTHUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0081-2 [15631008102]

BISMUTHUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

Drug Details

Active Ingredients

IngredientStrength
BISMUTH6 [hp_X]/1

OpenFDA Data

SPL SET ID:4a51c615-0e66-4cdb-a84c-5d2c7f9fb36b
Manufacturer
UNII

NDC Crossover Matching brand name "BISMUTHUM METALLICUM" or generic name "Bismuthum Metallicum"

NDCBrand NameGeneric Name
0220-0851Bismuthum metallicumBISMUTH
15631-0081BISMUTHUM METALLICUMBISMUTHUM METALLICUM
68428-258Bismuthum metallicumBISMUTH
71919-124Bismuthum metallicumBISMUTH

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