NDC 55714-6283

Iodium

Iodium

Iodium is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Newton Laboratories, Inc.. The primary component is Iodine.

Product ID55714-6283_d40d68f6-6763-50b4-deae-683607daca55
NDC55714-6283
Product TypeHuman Otc Drug
Proprietary NameIodium
Generic NameIodium
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNewton Laboratories, Inc.
Substance NameIODINE
Active Ingredient Strength15 [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 55714-6283-1

30 mL in 1 BOTTLE, GLASS (55714-6283-1)
Marketing Start Date2011-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55714-6283-1 [55714628301]

Iodium LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-09-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
IODINE15 [hp_X]/mL

OpenFDA Data

SPL SET ID:c7b2ec27-ef9c-94ca-82f5-a9c0af9dca92
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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