Home NDC 85816-5121 BM Berberis Vulgaris
Product NDC 85816-5121
11-digit product format 858165121
Labeler code 85816
Product ID 85816-5121_5ebffab5-95df-3f84-e063-6294a90af393
Type HUMAN OTC DRUG
Nonproprietary name Berberis Vulgaris
Dosage form TINCTURE
Route ORAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-01
Substance BERBERIS VULGARIS ROOT BARK
Active strength 1 [hp_X]/mL
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 BM Berberis Vulgaris
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BERBERIS VULGARIS ROOT BARK 1 [hp_X]/mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85816-5121-1 BM Berberis Vulgaris 30 mL in 1 BOTTLE, GLASS TINCTURE 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 85816-5121-1 85816512101 30 mL in 1 BOTTLE, GLASS (85816-5121-1) 30 ml 2015-01-01 No No Current