Home NDC 71919-819-01 Thiosinaminum
Product NDC 71919-819
Requested package NDC 71919-819-01
11-digit product format 719190819
Labeler code 71919
Product ID 71919-819_2cc890bb-e861-a6b1-e063-6394a90a494d
Type HUMAN OTC DRUG
Nonproprietary name ALLYLTHIOUREA
Dosage form PELLET
Route ORAL
Labeler Washington Homeopathic Products
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-11-08
Substance ALLYLTHIOUREA
Active strength 30 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 71919-819 71919-819-01 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 71919-819 71919-819-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Thiosinaminum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLYLTHIOUREA 30 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 706IDJ14B7 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 71919-819-01 Thiosinaminum 350 in 1 VIAL, GLASS PELLET 350 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71919-819 THIOSINAMINUM (ALLYLTHIOUREA) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS] 2 Current NDC, 1 package rows 20250130_09a60d62-a479-0f02-e063-6294a90a6d39.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 71919-819-01 71919081901 350 PELLET in 1 VIAL, GLASS (71919-819-01) 350 pellet 2023-11-08 No No Current