Home NDC 37662-4111 Titanium Muriaticum
Product NDC 37662-4111
11-digit product format 376624111
Labeler code 37662
Product ID 37662-4111_0715c85f-b4ee-cdb9-e063-6394a90a0507
Type HUMAN OTC DRUG
Nonproprietary name Titanium Muriaticum
Dosage form PELLET
Route ORAL
Labeler Hahnemann Laboratories, INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-10-06
Substance TITANIUM DICHLORIDE
Active strength 1 [hp_Q]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Titanium Muriaticum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DICHLORIDE 1 [hp_Q]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination BK26WI342Q 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 37662-4111-1 Titanium Muriaticum 10000 in 1 BOTTLE, GLASS PELLET 10000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37662-4111 TITANIUM MURIATICUM PELLET [HAHNEMANN LABORATORIES, INC.] 1 Current NDC, 1 package rows 20231007_0715c85f-b4ed-cdb9-e063-6394a90a0507.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 Units Marketing start Sample Exclude flag Status 37662-4111-1 37662411101 10000 PELLET in 1 BOTTLE, GLASS (37662-4111-1) 10000 pellet 2023-10-06 No No Current