Home NDC 0220-9089 ARNICA
Product NDC 0220-9089
11-digit product format 002209089
Labeler code 0220
Product ID 0220-9089_0682b0ee-eebc-c149-e063-6294a90a6293
Type HUMAN OTC DRUG
Nonproprietary name ARNICA MONTANA
Dosage form TABLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-10-01
Substance ARNICA MONTANA
Active strength 30 [hp_X]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base ARNICA
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 30 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O80TY208ZW 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 0220-9089-04 ARNICA 60 in 1 BLISTER PACK TABLET 60 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-9089 ARNICA (ARNICA MONTANA) TABLET [BOIRON] 1 Current NDC, 1 package rows 20231001_0682b0ee-eebb-c149-e063-6294a90a6293.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 Units Marketing start Sample Exclude flag Status 0220-9089-04 00220908904 60 TABLET in 1 BLISTER PACK (0220-9089-04) 60 tablet 2023-10-01 No No Current