Home NDC 82969-5226 BMNP AMBRA GRISEA
Product NDC 82969-5226
11-digit product format 829695226
Labeler code 82969
Product ID 82969-5226_5a69d7cd-7713-f9a0-e063-6294a90ae987
Type HUMAN OTC DRUG
Nonproprietary name AMBRA GRISEA
Dosage form GLOBULE
Route ORAL
Labeler Total Operations Management LLC DBA:Bestmade Natural Products Micro
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-06-01
Substance AMBERGRIS
Active strength 30 [hp_C]/g
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 BMNP AMBRA GRISEA
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMBERGRIS 30 [hp_C]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination XTC0D02P6C Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 82969-5226-1 82969522601 25 g in 1 BOTTLE, GLASS (82969-5226-1) 25 g 2026-06-01 No No Current 82969-5226-2 82969522602 8 g in 1 BOTTLE, GLASS (82969-5226-2) 8 g 2026-06-01 No No Current