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 ID: 55714-6283_d40d68f6-6763-50b4-deae-683607daca55
• NDC: 55714-6283
• Product Type: Human Otc Drug
• Proprietary Name: Iodium
• Generic Name: Iodium
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2011-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Newton Laboratories, Inc.
• Substance Name: IODINE
• Active Ingredient Strength: 15 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 55714-6283-1

30 mL in 1 BOTTLE, GLASS (55714-6283-1)

• Marketing Start Date: 2011-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55714-6283-1 [55714628301]

Iodium LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-09-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
IODINE	15 [hp_X]/mL

OpenFDA Data

• SPL SET ID: c7b2ec27-ef9c-94ca-82f5-a9c0af9dca92
• Manufacturer:
  • Newton Laboratories, Inc.
• UNII:
  • 9679TC07X4

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

NDC	Brand Name	Generic Name
0220-2656	Iodium	IODINE
0220-2657	Iodium	IODINE
0220-2659	Iodium	IODINE
0220-2661	Iodium	IODINE
0220-2664	Iodium	IODINE
0220-2673	Iodium	IODINE
0220-2674	Iodium	IODINE
15631-0236	IODIUM	IODIUM
37662-1714	Iodium	Iodium
37662-1715	Iodium	Iodium
37662-1716	Iodium	Iodium
37662-1717	Iodium	Iodium
37662-1718	Iodium	Iodium
37662-1719	Iodium	Iodium
37662-1720	Iodium	Iodium
37662-1721	Iodium	Iodium
37662-1722	Iodium	Iodium
53645-2120	Iodium	Iodium
55714-6283	Iodium	Iodium
62106-5070	IODIUM	Iodine
68428-440	Iodium	IODINE
71919-364	Iodium	IODINE
43857-0088	Bio Iodine	Iodium
69152-1206	Iodium 6C	Iodium