Home NDC 85816-5117 BM Baptisia Tinctoria
Product NDC 85816-5117
11-digit product format 858165117
Labeler code 85816
Product ID 85816-5117_5c571698-cb2d-660d-e063-6394a90aebeb
Type HUMAN OTC DRUG
Nonproprietary name Baptisia Tinctoria
Dosage form GLOBULE
Route ORAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-01
Substance BAPTISIA TINCTORIA
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 Baptisia Tinctoria
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BAPTISIA TINCTORIA 30 [hp_C]/1000mg
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85816-5117-1 BM Baptisia Tinctoria 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 85816-5117-1 85816511701 30000 mg in 1 BOTTLE, GLASS (85816-5117-1) 30000 mg 2015-01-01 No No Current