Home NDC 85816-5106 BM Digitalis Purpurea
Product NDC 85816-5106
11-digit product format 858165106
Labeler code 85816
Product ID 85816-5106_5c56cf6e-7266-7848-e063-6294a90ab347
Type HUMAN OTC DRUG
Nonproprietary name Digitalis Purpurea
Dosage form GLOBULE
Route ORAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-01
Substance DIGITALIS
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 Digitalis Purpurea
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIGITALIS 30 [hp_C]/1000mg
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85816-5106-1 BM Digitalis Purpurea 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 85816-5106-1 85816510601 30000 mg in 1 BOTTLE, GLASS (85816-5106-1) 30000 mg 2015-01-01 No No Current