NDC 15631-0236

IODIUM

Iodium

IODIUM 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 Iodine.

Product ID15631-0236_08031370-d152-409e-91ac-623b06fee32f
NDC15631-0236
Product TypeHuman Otc Drug
Proprietary NameIODIUM
Generic NameIodium
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 NameIODINE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0236-0

100 PELLET in 1 PACKAGE (15631-0236-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0236-1 [15631023601]

IODIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0236-0 [15631023600]

IODIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0236-2 [15631023602]

IODIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0236-4 [15631023604]

IODIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0236-3 [15631023603]

IODIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0236-5 [15631023605]

IODIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
IODINE3 [hp_X]/1

OpenFDA Data

SPL SET ID:e7e33f04-b6ba-420e-9b0e-67c409c60d8f
Manufacturer
UNII

NDC Crossover Matching brand name "IODIUM" or generic name "Iodium"

NDCBrand NameGeneric Name
0220-2656IodiumIODINE
0220-2657IodiumIODINE
0220-2659IodiumIODINE
0220-2661IodiumIODINE
0220-2664IodiumIODINE
0220-2673IodiumIODINE
0220-2674IodiumIODINE
15631-0236IODIUMIODIUM
37662-1714IodiumIodium
37662-1715IodiumIodium
37662-1716IodiumIodium
37662-1717IodiumIodium
37662-1718IodiumIodium
37662-1719IodiumIodium
37662-1720IodiumIodium
37662-1721IodiumIodium
37662-1722IodiumIodium
53645-2120IodiumIodium
55714-6283IodiumIodium
62106-5070IODIUMIodine
68428-440IodiumIODINE
71919-364IodiumIODINE
43857-0088Bio IodineIodium
69152-1206Iodium 6CIodium

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