Home NDC 0220-9023 Arnicare
Product NDC 0220-9023
11-digit product format 002209023
Labeler code 0220
Product ID 0220-9023_29f6e606-cfe1-4ca1-e063-6294a90a9456
Type HUMAN OTC DRUG
Nonproprietary name ARNICA MONTANA
Dosage form OINTMENT
Route CUTANEOUS
Labeler Laboratoires Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2007-06-02
Substance ARNICA MONTANA
Active strength 1 [hp_X]/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Arnicare
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 1 [hp_X]/g
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 0220-9023-51 Arnicare 30 g in 1 BOX OINTMENT 30 7
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-9023 ARNICARE (ARNICA MONTANA) OINTMENT [LABORATOIRES BOIRON] 7 Current NDC, Legacy NDC, 1 package rows 20241228_9d03bd9c-ab1e-4414-afd2-8f9c80000164.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 Marketing end Sample Exclude flag Status 0220-9023-51 00220902351 30 g in 1 BOX (0220-9023-51) 30 g 2007-06-02 0000-00-00 No No Current