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United States · US · US:0220-9059_30d0f65b-a256-29b9-e063-6394a90a9b0f
Arnicare Arnica
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLaboratoires Boiron
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11022090590460 TABLET in 1 BLISTER PACK (0220-9059-04)
- ndc110220905929120 TABLET in 1 BLISTER PACK (0220-9059-29)
- ndc110220905992100 TABLET in 1 BLISTER PACK (0220-9059-92)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "ORAL",
"spl_meta": {
"b957a592-e51b-61fc-e053-2995a90aaabd": {
"match": "brand_token",
"title": "ARNICARE BRUISE (ARNICA MONTANA) CREAM [BOIRON]",
"spl_version": "9",
"published_date": "2026-05-21"
}
},
"productid": "0220-9059_30d0f65b-a256-29b9-e063-6394a90a9b0f",
"productndc": "0220-9059",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ARNICA MONTANA",
"proprietary_name": "Arnicare Arnica",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "ARNICA MONTANA",
"start_marketing_date": "20110711",
"active_numerator_strength": "9"
}Access this data programmatically
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