Arnicare Procedure Recovery

Product NDC
0220-9050
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0508-41Arnicare Procedure Recovery80 in 1 TUBEPELLET330 [hp_C]8
0220-9050-75Arnicare Procedure Recovery1 in 1 PACKAGEKIT18

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9050ARNICARE PROCEDURE RECOVERY (ARNICA MONTANA) KIT [LABORATOIRES BOIRON]7Current NDC, Legacy NDC, 2 package rows20230106_f0003627-b81c-46b6-8773-4f2987b75739.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0220-0508-410022005084180 in 1 TUBEHistorical
0220-9050-75002209050751 KIT in 1 PACKAGE (0220-9050-75) * 80 PELLET in 1 TUBE (0220-0508-41) 1 kit2007-11-010000-00-00NoNoCurrent