NDC 0220-4837

Sulphur iodatum

Sulfur Iodide

Sulphur iodatum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Laboratoires Boiron. The primary component is Sulfur Iodide.

• Product ID: 0220-4837_6011e637-57f2-1e67-e053-2991aa0a3374
• NDC: 0220-4837
• Product Type: Human Otc Drug
• Proprietary Name: Sulphur iodatum
• Generic Name: Sulfur Iodide
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Laboratoires Boiron
• Substance Name: SULFUR IODIDE
• Active Ingredient Strength: 6 [hp_C]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-4837-41

80 PELLET in 1 TUBE (0220-4837-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-4837-41 [00220483741]

Sulphur iodatum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
SULFUR IODIDE	6 [hp_C]/1

OpenFDA Data

• SPL SET ID: 67261e30-7c2e-11e6-87ed-424c58303031
• Manufacturer:
  • Laboratoires Boiron
• 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