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United States · US · US:0220-9000_3a728515-f1d3-bcb9-e063-6294a90a4910

Arnicare

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 · 8

  • ndc11
    0220900054
    1 TUBE in 1 PACKAGE (0220-9000-54) / 45 g in 1 TUBE
  • ndc11
    0220900059
    1 TUBE in 1 PACKAGE (0220-9000-59) / 75 g in 1 TUBE
  • ndc11
    0220900065
    1 TUBE in 1 PACKAGE (0220-9000-65) / 14 g in 1 TUBE
  • ndc11
    0220900066
    1 TUBE in 1 PACKAGE (0220-9000-66) / 120 g in 1 TUBE
  • ndc11
    0220900084
    1 TUBE in 1 PACKAGE (0220-9000-84) / 45 g in 1 TUBE
  • ndc11
    0220900085
    2 TUBE in 1 PACKAGE (0220-9000-85) / 120 g in 1 TUBE
  • ndc11
    0220900086
    2 TUBE in 1 PACKAGE (0220-9000-86) / 45 g in 1 TUBE
  • ndc11
    0220900094
    5 g in 1 POUCH (0220-9000-94)

Annotations

DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "route": "TOPICAL",
  "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": "0220-9000_3a728515-f1d3-bcb9-e063-6294a90a4910",
  "productndc": "0220-9000",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ARNICA MONTANA",
  "proprietary_name": "Arnicare",
  "active_ingred_unit": "[hp_X]/g",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "ARNICA MONTANA",
  "start_marketing_date": "20070109",
  "active_numerator_strength": "1"
}

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