NDC 62106-5318

SULPHUR IODATUM

Sulfur Iodide

SULPHUR IODATUM is a Oral Granule in the Human Otc Drug category. It is labeled and distributed by Seroyal Usa. The primary component is Sulfur Iodide.

• Product ID: 62106-5318_1aefe34f-85b7-20f9-e054-00144ff88e88
• NDC: 62106-5318
• Product Type: Human Otc Drug
• Proprietary Name: SULPHUR IODATUM
• Generic Name: Sulfur Iodide
• Dosage Form: Granule
• Route of Administration: ORAL
• Marketing Start Date: 2015-07-15
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Seroyal USA
• Substance Name: SULFUR IODIDE
• Active Ingredient Strength: 3 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 62106-5318-4

10 TUBE in 1 CARTON (62106-5318-4) > 140 GRANULE in 1 TUBE

• Marketing Start Date: 2015-07-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 62106-5318-4 [62106531804]

SULPHUR IODATUM GRANULE

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-07-15

Drug Details

Active Ingredients

Ingredient	Strength
SULFUR IODIDE	3 [hp_X]/1

OpenFDA Data

• SPL SET ID: 1aefe34f-85b6-20f9-e054-00144ff88e88
• Manufacturer:
  • Seroyal USA
• UNII:
  • L6L8KA2AA0

NDC Crossover Matching brand name "SULPHUR IODATUM" or generic name "Sulfur Iodide"

NDC	Brand Name	Generic Name
0220-4834	Sulphur iodatum	SULFUR IODIDE
0220-4835	Sulphur iodatum	SULFUR IODIDE
0220-4837	Sulphur iodatum	SULFUR IODIDE
0220-4839	SULPHUR IODATUM	SULFUR IODIDE
0220-4842	Sulphur iodatum	SULFUR IODIDE
0220-4843	Sulphur iodatum	SULFUR IODIDE
15631-0421	SULPHUR IODATUM	SULPHUR IODATUM
62106-5318	SULPHUR IODATUM	Sulfur iodide
68428-656	Sulphur iodatum	SULFUR IODIDE
71919-655	SULPHUR IODATUM	Ssulfur iodide
64117-188	Acne Skin eruptions	SULFUR IODIDE