Home NDC 0220-9050-75 Arnicare Procedure Recovery
Product NDC 0220-9050
Requested package NDC 0220-9050-75
11-digit product format 002209050
Labeler code 0220
Product ID 0220-9050_4b725efe-d109-8e9f-e063-6294a90aeaaa
Type HUMAN OTC DRUG
Nonproprietary name ARNICA MONTANA
Dosage form KIT
Route ORAL
Labeler Laboratoires Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2007-11-01
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Arnicare Procedure Recovery
Listing expiration 2027-12-31 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 0220-0508-41 Arnicare Procedure Recovery 80 in 1 TUBE PELLET 3 30 [hp_C] 8 0220-9050-75 Arnicare Procedure Recovery 1 in 1 PACKAGE KIT 1 8
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-9050 ARNICARE PROCEDURE RECOVERY (ARNICA MONTANA) KIT [LABORATOIRES BOIRON] 7 Current NDC, Legacy NDC, 2 package rows 20230106_f0003627-b81c-46b6-8773-4f2987b75739.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 0220-9050-75 00220905075 1 KIT in 1 PACKAGE (0220-9050-75) * 80 PELLET in 1 TUBE (0220-0508-41) 1 kit 2007-11-01 0000-00-00 No No Current