NDC 0220-2673

Iodium

Iodine

Iodium is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Iodine.

Product ID0220-2673_85cd0c27-785a-5fd8-e053-2a91aa0a7c69
NDC0220-2673
Product TypeHuman Otc Drug
Proprietary NameIodium
Generic NameIodine
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date1983-03-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameBoiron
Substance NameIODINE
Active Ingredient Strength15 [hp_C]/15[hp_C]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0220-2673-41

15 [hp_C] in 1 TUBE (0220-2673-41)
Marketing Start Date1983-03-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0220-2673-41 [00220267341]

Iodium PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1983-03-03

Drug Details

Active Ingredients

IngredientStrength
IODINE15 [hp_C]/15[hp_C]

OpenFDA Data

SPL SET ID:85cd0c27-7859-5fd8-e053-2a91aa0a7c69
Manufacturer
UNII

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

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
68428-440IodiumIodium
71919-364IodiumIodium
43857-0088Bio IodineIodium
64117-148Dry CoughIODINE
0363-0088IodineIodine
0869-0088IodineIodine
11344-088IodineIodine
41163-088IodineIodine
50804-088IodineIodine
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