Home NDC 0220-6535 Crataegus
Product NDC 0220-6535
11-digit product format 002206535
Labeler code 0220
Product ID 0220-6535_08693119-e5fa-6f91-e063-6394a90a3022
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name HAWTHORN LEAF WITH FLOWER
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance HAWTHORN LEAF WITH FLOWER
Active strength 6 [hp_X]/6[hp_X]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Crataegus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HAWTHORN LEAF WITH FLOWER 6 [hp_X]/6[hp_X]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 6OM09RPY36 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 0220-6535-41 Crataegus 6 [hp_X] in 1 TUBE PELLET 6 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-6535 CRATAEGUS (HAWTHORN LEAF WITH FLOWER ) PELLET [BOIRON] 3 Current NDC, Legacy NDC, 1 package rows 20231024_8735a526-67e2-12ac-e053-2991aa0a793e.zip
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 Marketing start Marketing end Sample Exclude flag Status 0220-6535-41 00220653541 6 [hp_X] in 1 TUBE (0220-6535-41) 1983-03-03 0000-00-00 No No Current