Home NDC 85816-5123 BM Crataegus Oxy
Product NDC 85816-5123
11-digit product format 858165123
Labeler code 85816
Product ID 85816-5123_38db86ca-917f-d6b4-e063-6294a90a0cc7
Type HUMAN OTC DRUG
Nonproprietary name Crataegus Oxy
Dosage form TINCTURE
Route ORAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-01
Substance CRATAEGUS FRUIT
Active strength 1 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base BM Crataegus Oxy
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CRATAEGUS FRUIT 1 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination Q21UUL2105 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85816-5123-1 BM Crataegus Oxy 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 85816-5123-1 85816512301 30 mL in 1 BOTTLE, GLASS (85816-5123-1) 30 ml 2015-01-01 No No Current