Home NDC 0220-0230 AMBROSIA ARTEMISIAEFOLIA
Product NDC 0220-0230
11-digit product format 002200230
Labeler code 0220
Product ID 0220-0230_0c069179-fc7d-cf6b-e063-6394a90aeaeb
Type HUMAN OTC DRUG
Nonproprietary name AMBROSIA ARTEMISIIFOLIA
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-01-01
Substance AMBROSIA ARTEMISIIFOLIA
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 AMBROSIA ARTEMISIAEFOLIA
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMBROSIA ARTEMISIIFOLIA 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 9W34L2CQ9A 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 0220-0230-41 AMBROSIA ARTEMISIAEFOLIA 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 0220-0230 AMBROSIA ARTEMISIAEFOLIA (AMBROSIA ARTEMISIIFOLIA) PELLET [BOIRON] 1 Current NDC, 1 package rows 20240101_0c069179-fc7c-cf6b-e063-6394a90aeaeb.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 0220-0230-41 00220023041 200 [kp_C] in 1 TUBE (0220-0230-41) 2024-01-01 No No Current