NDC 15631-0064

AURUM IODATUM

Aurum Iodatum

AURUM 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 Gold Monoiodide.

Product ID15631-0064_9045d1f8-d790-4ab8-aba8-0f907422f4ea
NDC15631-0064
Product TypeHuman Otc Drug
Proprietary NameAURUM IODATUM
Generic NameAurum Iodatum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-12
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameGOLD MONOIODIDE
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0064-0

100 PELLET in 1 PACKAGE (15631-0064-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0064-2 [15631006402]

AURUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0064-0 [15631006400]

AURUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0064-5 [15631006405]

AURUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0064-3 [15631006403]

AURUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0064-4 [15631006404]

AURUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0064-1 [15631006401]

AURUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

Drug Details

Active Ingredients

IngredientStrength
GOLD MONOIODIDE6 [hp_X]/1

OpenFDA Data

SPL SET ID:68a3708a-c14d-426a-a02a-3b3cde779e24
Manufacturer
UNII

NDC Crossover Matching brand name "AURUM IODATUM" or generic name "Aurum Iodatum"

NDCBrand NameGeneric Name
0220-0630Aurum iodatumGOLD MONOIODIDE
0220-0632Aurum iodatumGOLD MONOIODIDE
15631-0064AURUM IODATUMAURUM IODATUM
68428-239Aurum iodatumGOLD MONOIODIDE
71919-100Aurum iodatumGOLD MONOIODIDE

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