Home NDC 85816-5050 BM Dulcamara
Product NDC 85816-5050
11-digit product format 858165050
Labeler code 85816
Product ID 85816-5050_5c5610f4-7823-fbfa-e063-6294a90a1a20
Type HUMAN OTC DRUG
Nonproprietary name Dulcamara
Dosage form GLOBULE
Route ORAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-01
Substance SOLANUM DULCAMARA FLOWER
Active strength 30 [hp_C]/1000mg
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 Dulcamara
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SOLANUM DULCAMARA FLOWER 30 [hp_C]/1000mg
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85816-5050-1 BM Dulcamara 30000 mg in 1 BOTTLE, GLASS GLOBULE 30000 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 85816-5050-1 85816505001 30000 mg in 1 BOTTLE, GLASS (85816-5050-1) 30000 mg 2015-01-01 No No Current