Home NDC 82969-5125 Thuja Occ CM
Product NDC 82969-5125
11-digit product format 829695125
Labeler code 82969
Product ID 82969-5125_36d55db8-48fb-8afd-e063-6394a90a6540
Type HUMAN OTC DRUG
Nonproprietary name Thuja Occidentalis CM (HPUS)
Dosage form LIQUID
Route ORAL
Labeler Bestmade Natural Products
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-06-01
Substance THUJA OCCIDENTALIS LEAFY TWIG
Active strength 100000 [hp_C]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Thuja Occ CM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength THUJA OCCIDENTALIS LEAFY TWIG 100000 [hp_C]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1NT28V9397 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 82969-5125-1 Thuja Occ CM 30 mL in 1 BOTTLE, GLASS LIQUID 30 1
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 82969-5125-1 82969512501 30 mL in 1 BOTTLE, GLASS (82969-5125-1) 30 ml 2025-06-01 No No Current