Home NDC 0220-4839 SULPHUR IODATUM
Product NDC 0220-4839
11-digit product format 002204839
Labeler code 0220
Product ID 0220-4839_0a3421ae-8d23-3d0b-e063-6394a90ad467
Type HUMAN OTC DRUG
Nonproprietary name SULFUR IODIDE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance SULFUR IODIDE
Active strength 200 [kp_C]/200[kp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base SULPHUR IODATUM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR IODIDE 200 [kp_C]/200[kp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L6L8KA2AA0 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-4839-41 SULPHUR IODATUM 200 [kp_C] in 1 TUBE PELLET 200 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-4839 SULPHUR IODATUM (SULFUR IODIDE) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20231116_86935e36-ab98-b8d1-e053-2a91aa0ab0b6.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0220-4839-41 00220483941 200 [kp_C] in 1 TUBE (0220-4839-41) 1983-03-03 0000-00-00 No No Current