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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

  • ndc11
    0220905904
    60 TABLET in 1 BLISTER PACK (0220-9059-04)
  • ndc11
    0220905929
    120 TABLET in 1 BLISTER PACK (0220-9059-29)
  • ndc11
    0220905992
    100 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"
}

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