FDA.reportPublic FDA data

Arnicare Bruise

Product NDC
0220-9084
11-digit product format
002209084
Labeler code
0220
Product ID
0220-9084_3054e90d-d3f8-b5f5-e063-6294a90ae056
Type
HUMAN OTC DRUG
Nonproprietary name
ARNICA MONTANA
Dosage form
GEL
Route
TOPICAL
Labeler
Laboratoires Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2016-02-01
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 Bruise
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA1 [hp_X]/g

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
9d86cfb0-e155-4b0f-8bd0-ad5e8a335707Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-9084-542023-02-21C16284748780-1f386c649-c27c-0266-e053-dadaa90a7c1aArnicare Bruise
0220-9084-542023-01-30C16284748780-1f386c649-c27c-0266-e053-dadaa90a7c1aArnicare Bruise

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9084-54Arnicare Bruise1 in 1 PACKAGEGEL19
0220-9084-54Arnicare Bruise45 g in 1 TUBEGEL459
0220-9084-59Arnicare Bruise1 in 1 CARTONGEL19
0220-9084-59Arnicare Bruise75 g in 1 TUBEGEL759
0220-9084-66Arnicare Bruise120 g in 1 TUBEGEL1209
0220-9084-66Arnicare Bruise1 in 1 CARTONGEL19

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0220-9084-54GM - Gram0220-908410be5049-5d08-45d7-abcf-bb741113f1c212021-02-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9084ARNICARE BRUISE (ARNICA MONTANA) GEL [LABORATOIRES BOIRON]9Current NDC, Legacy NDC, 6 package rows20250316_9d86cfb0-e155-4b0f-8bd0-ad5e8a335707.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 BruiseARNICA MONTANALaboratoires Boiron9d86cfb0-e155-4b0f-8bd0-ad5e8a3357072025-03-14WarningsExact identifier
ndc (product): 0220-9084

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0220-9084-54002209084541 TUBE in 1 PACKAGE (0220-9084-54) / 45 g in 1 TUBE1 tube2016-02-010000-00-00NoNoCurrent
0220-9084-59002209084591 TUBE in 1 CARTON (0220-9084-59) / 75 g in 1 TUBE1 tube2024-12-27NoNoCurrent
0220-9084-66002209084661 TUBE in 1 CARTON (0220-9084-66) / 120 g in 1 TUBE1 tube2024-12-27NoNoCurrent