NDC 0220-4835

Sulphur iodatum

Sulfur Iodide

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

• Product ID: 0220-4835_8693d143-14d2-5272-e053-2991aa0a2e6c
• NDC: 0220-4835
• 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: Boiron
• Substance Name: SULFUR IODIDE
• Active Ingredient Strength: 12 [hp_C]/12[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0220-4835-41

12 [hp_C] in 1 TUBE (0220-4835-41)

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

NDC SPL Data Element Entries

NDC 0220-4835-41 [00220483541]

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	12 [hp_C]/12[hp_C]

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