Home NDC 0220-5031 Titanium metallicum
Product NDC 0220-5031
11-digit product format 002205031
Labeler code 0220
Product ID 0220-5031_21b504bc-e12e-3a8e-e063-6294a90a7708
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-01-01
Substance TITANIUM
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 Titanium metallicum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM 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 D1JT611TNE 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 0220-5031-41 Titanium metallicum 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 0220-5031 TITANIUM METALLICUM (TITANIUM) PELLET [BOIRON] 1 Current NDC, 1 package rows 20240910_21b504bc-e12d-3a8e-e063-6294a90a7708.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 0220-5031-41 00220503141 200 [kp_C] in 1 TUBE (0220-5031-41) 2024-01-01 No No Current