Home NDC 0220-0572 Asafoetida
Product NDC 0220-0572
11-digit product format 002200572
Labeler code 0220
Product ID 0220-0572_253f4bc7-0144-ab66-e063-6294a90a89c5
Type HUMAN OTC DRUG
Nonproprietary name FERULA ASSA-FOETIDA RESIN
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance FERULA ASSA-FOETIDA RESIN
Active strength 3 [hp_X]/3[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 Asafoetida
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FERULA ASSA-FOETIDA RESIN 3 [hp_X]/3[hp_X]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination W9FZA51AS1 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-0572-41 Asafoetida 3 [hp_X] in 1 TUBE PELLET 3 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-0572 ASAFOETIDA (FERULA ASSA-FOETIDA RESIN ) PELLET [BOIRON] 3 Current NDC, Legacy NDC, 1 package rows 20241027_8733c4a0-3fa3-83b3-e053-2991aa0afe58.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 0220-0572-41 00220057241 3 [hp_X] in 1 TUBE (0220-0572-41) 1983-03-03 0000-00-00 No No Current