Home NDC 0220-4831-41 Sulphur
Product NDC 0220-4831
Requested package NDC 0220-4831-41
11-digit product format 002204831
Labeler code 0220
Product ID 0220-4831_f67ce46f-fe85-e06f-e053-2a95a90ae28d
Type HUMAN OTC DRUG
Nonproprietary name SULFUR
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance SULFUR
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
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 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 70FD1KFU70 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 0220-4831-41 Sulphur 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 0220-4831 SULPHUR (SULFUR) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230310_8696ff13-5c36-0ecc-e053-2991aa0aff62.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 0220-4831-41 00220483141 200 [kp_C] in 1 TUBE (0220-4831-41) 1983-03-03 0000-00-00 No No Current