Home NDC 85816-5125 BM Thuja Occ
Product NDC 85816-5125
11-digit product format 858165125
Labeler code 85816
Product ID 85816-5125_38dde5f0-fed3-d113-e063-6294a90abb44
Type HUMAN OTC DRUG
Nonproprietary name Thuja Occidentalis
Dosage form LIQUID
Route ORAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-01
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 BM Thuja Occ
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 85816-5125-1 BM Thuja Occ 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 85816-5125-1 85816512501 30 mL in 1 BOTTLE, GLASS (85816-5125-1) 30 ml 2015-01-01 No No Current