Home NDC 0220-3389 Mercurius sulphuratus ruber
Product NDC 0220-3389
11-digit product format 002203389
Labeler code 0220
Product ID 0220-3389_202328e9-612a-8bc4-e063-6394a90a827e
Type HUMAN OTC DRUG
Nonproprietary name MERCURIC SULFIDE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-01-01
Substance MERCURIC SULFIDE
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 Mercurius sulphuratus ruber
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MERCURIC SULFIDE 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 ZI0T668SF1 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-3389-41 Mercurius sulphuratus ruber 200 [kp_C] in 1 TUBE PELLET 200 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-3389 MERCURIUS SULPHURATUS RUBER (MERCURIC SULFIDE) PELLET [BOIRON] 1 Current NDC, 1 package rows 20240822_202328e9-6129-8bc4-e063-6394a90a827e.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 Sample Exclude flag Status 0220-3389-41 00220338941 200 [kp_C] in 1 TUBE (0220-3389-41) 2024-01-01 No No Current