FDA.reportPublic FDA data

Arnicare Arnica

Product NDC
0220-9059
11-digit product format
002209059
Labeler code
0220
Product ID
0220-9059_30d0f65b-a256-29b9-e063-6394a90a9b0f
Type
HUMAN OTC DRUG
Nonproprietary name
ARNICA MONTANA
Dosage form
TABLET
Route
ORAL
Labeler
Laboratoires Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-07-11
Substance
ARNICA MONTANA
Active strength
9 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Arnicare Arnica
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA9 [hp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O80TY208ZWInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
96a3e7ea-94ed-46b4-94d7-70b8cc68c688Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
0220-9059-042023-07-18Arnicare Tablets
0220-9059-292023-07-18Arnicare Tablets
0220-9059-042023-01-30Arnicare Tablets
0220-9059-292023-01-30Arnicare Tablets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9059-04Arnicare Arnica60 in 1 BLISTER PACKTABLET6010
0220-9059-29Arnicare Arnica120 in 1 BLISTER PACKTABLET12010
0220-9059-92Arnicare Arnica100 in 1 BLISTER PACKTABLET10010

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0220-9059-04EA - Each0220-905937f517f3-3f9e-4dc3-9755-0d3a4535dbb512021-02-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZWARNICARE ARNICA (ARNICA MONTANA) TABLET [LABORATOIRES BOIRON]4
ARNICA MONTANAACTIVE MOIETYO80TY208ZWARNICARE ARNICA (ARNICA MONTANA) TABLET [LABORATOIRES BOIRON]4
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48ARNICARE ARNICA (ARNICA MONTANA) TABLET [LABORATOIRES BOIRON]4
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GARNICARE ARNICA (ARNICA MONTANA) TABLET [LABORATOIRES BOIRON]4
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30ARNICARE ARNICA (ARNICA MONTANA) TABLET [LABORATOIRES BOIRON]4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9059ARNICARE ARNICA (ARNICA MONTANA) TABLET [LABORATOIRES BOIRON]10Current NDC, Legacy NDC, 3 package rows20250323_96a3e7ea-94ed-46b4-94d7-70b8cc68c688.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 ArnicaARNICA MONTANALaboratoires Boiron96a3e7ea-94ed-46b4-94d7-70b8cc68c6882025-03-20Exact identifier
ndc (product): 0220-9059

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0220-9059-040022090590460 TABLET in 1 BLISTER PACK (0220-9059-04) 60 tablet2011-07-110000-00-00NoNoCurrent
0220-9059-2900220905929120 TABLET in 1 BLISTER PACK (0220-9059-29) 120 tablet2021-04-090000-00-00NoNoCurrent
0220-9059-9200220905992100 TABLET in 1 BLISTER PACK (0220-9059-92) 100 tablet2025-03-20NoNoCurrent