Home NDC 82969-5123 Crataegus Oxy
Product NDC 82969-5123
11-digit product format 829695123
Labeler code 82969
Product ID 82969-5123_36d4496c-297f-520d-e063-6294a90ab458
Type HUMAN OTC DRUG
Nonproprietary name Crataegus Oxyacantha (HPUS)
Dosage form TINCTURE
Route ORAL
Labeler Bestmade Natural Products
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-06-01
Substance CRATAEGUS FRUIT
Active strength 1 [hp_M]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Crataegus Oxy
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CRATAEGUS FRUIT 1 [hp_M]/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 82969-5123-1 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 82969-5123-1 82969512301 30 mL in 1 BOTTLE, GLASS (82969-5123-1) 30 ml 2025-06-01 No No Current