Home NDC 53645-1232 Thyroidinum 20X
Product NDC 53645-1232
11-digit product format 536451232
Labeler code 53645
Product ID 53645-1232_5724cb83-2111-5fb2-e063-6294a90aa206
Type HUMAN OTC DRUG
Nonproprietary name Thyroidinum 20X
Dosage form LIQUID
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-07-21
Substance THYROID, BOVINE
Active strength 20 [hp_X]/30mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Thyroidinum 20X
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength THYROID, BOVINE 20 [hp_X]/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination MN18OTN73W Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 53645-1232-6 53645123206 30 mL in 1 BOTTLE (53645-1232-6) 30 ml 2026-07-21 No No Current