FDA.reportPublic FDA data

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

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

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.

Identifier, FDA.report destination table
IdentifierFDA.report destination
f0003627-b81c-46b6-8773-4f2987b75739Available on FDA.report

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#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZWARNICARE PROCEDURE RECOVERY (ARNICA MONTANA) KIT [LABORATOIRES BOIRON]3
ARNICA MONTANAACTIVE MOIETYO80TY208ZWARNICARE PROCEDURE RECOVERY (ARNICA MONTANA) KIT [LABORATOIRES BOIRON]3
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GARNICARE PROCEDURE RECOVERY (ARNICA MONTANA) KIT [LABORATOIRES BOIRON]3
SUCROSEINACTIVE INGREDIENTC151H8M554ARNICARE PROCEDURE RECOVERY (ARNICA MONTANA) KIT [LABORATOIRES BOIRON]3

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

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Arnicare Procedure RecoveryARNICA MONTANALaboratoires Boironf0003627-b81c-46b6-8773-4f2987b757392026-02-22Exact identifier
ndc (package): 0220-9050-75
ndc (product): 0220-9050
ndc11 (package): 00220905075

Packages#

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