NDC 15631-0421

SULPHUR IODATUM

Sulphur Iodatum

SULPHUR IODATUM 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 Sulfur Iodide.

Product ID15631-0421_a1c3ae16-1ca7-767b-e053-2995a90aaed5
NDC15631-0421
Product TypeHuman Otc Drug
Proprietary NameSULPHUR IODATUM
Generic NameSulphur Iodatum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameSULFUR IODIDE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0421-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0421-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0421-2 [15631042102]

SULPHUR IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0421-3 [15631042103]

SULPHUR IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0421-4 [15631042104]

SULPHUR IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0421-0 [15631042100]

SULPHUR IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0421-5 [15631042105]

SULPHUR IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0421-1 [15631042101]

SULPHUR IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
SULFUR IODIDE3 [hp_X]/1

OpenFDA Data

SPL SET ID:a0ddcea2-94c8-4f5f-824c-90bb5b83b365
Manufacturer
UNII

NDC Crossover Matching brand name "SULPHUR IODATUM" or generic name "Sulphur Iodatum"

NDCBrand NameGeneric Name
0220-4834Sulphur iodatumSULFUR IODIDE
0220-4835Sulphur iodatumSULFUR IODIDE
0220-4837Sulphur iodatumSULFUR IODIDE
0220-4839SULPHUR IODATUMSULFUR IODIDE
0220-4842Sulphur iodatumSULFUR IODIDE
0220-4843Sulphur iodatumSULFUR IODIDE
15631-0421SULPHUR IODATUMSULPHUR IODATUM
62106-5318SULPHUR IODATUMSulfur iodide
68428-656Sulphur iodatumSULFUR IODIDE
71919-655SULPHUR IODATUMSsulfur iodide

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