Home NDC 0220-0003 ABELMOSCHUS
Product NDC 0220-0003
11-digit product format 002200003
Labeler code 0220
Product ID 0220-0003_079d9002-6f1c-efe6-e063-6394a90a70ba
Type HUMAN OTC DRUG
Nonproprietary name ABELMOSCHUS MOSCHATUS SEED
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-01-01
Substance ABELMOSCHUS MOSCHATUS SEED
Active strength 200 [kp_C]/200[kp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base ABELMOSCHUS
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ABELMOSCHUS MOSCHATUS SEED 200 [kp_C]/200[kp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination UN2QZ55I88 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 0220-0003-41 ABELMOSCHUS 200 [kp_C] in 1 TUBE PELLET 200 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-0003 ABELMOSCHUS (ABELMOSCHUS MOSCHATUS SEED) PELLET [BOIRON] 1 Current NDC, 1 package rows 20240101_079d9002-6f1b-efe6-e063-6394a90a70ba.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 Sample Exclude flag Status 0220-0003-41 00220000341 200 [kp_C] in 1 TUBE (0220-0003-41) 2024-01-01 No No Current