NDC 15631-0314

NICCOLUM SULPHURICUM

Niccolum Sulphuricum

NICCOLUM SULPHURICUM 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 Nickel Sulfate Hexahydrate.

Product ID15631-0314_a199c8a3-0b3a-4a79-e053-2995a90a9d2f
NDC15631-0314
Product TypeHuman Otc Drug
Proprietary NameNICCOLUM SULPHURICUM
Generic NameNiccolum Sulphuricum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameNICKEL SULFATE HEXAHYDRATE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0314-0

100 PELLET in 1 PACKAGE (15631-0314-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0314-5 [15631031405]

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

NDC 15631-0314-0 [15631031400]

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

NDC 15631-0314-3 [15631031403]

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

NDC 15631-0314-1 [15631031401]

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

NDC 15631-0314-4 [15631031404]

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

NDC 15631-0314-2 [15631031402]

NICCOLUM SULPHURICUM 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
NICKEL SULFATE HEXAHYDRATE3 [hp_X]/1

OpenFDA Data

SPL SET ID:da3902f7-e260-48d0-9c06-69081e6d6597
Manufacturer
UNII

NDC Crossover Matching brand name "NICCOLUM SULPHURICUM" or generic name "Niccolum Sulphuricum"

NDCBrand NameGeneric Name
15631-0314NICCOLUM SULPHURICUMNICCOLUM SULPHURICUM
37662-1162Niccolum SulphuricumNiccolum Sulphuricum
37662-1163Niccolum SulphuricumNiccolum Sulphuricum
37662-1164Niccolum SulphuricumNiccolum Sulphuricum
37662-1165Niccolum SulphuricumNiccolum Sulphuricum
37662-1166Niccolum SulphuricumNiccolum Sulphuricum
37662-1167Niccolum SulphuricumNiccolum Sulphuricum
37662-1168Niccolum SulphuricumNiccolum Sulphuricum

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