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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
- ndc1102209000541 TUBE in 1 PACKAGE (0220-9000-54) / 45 g in 1 TUBE
- ndc1102209000591 TUBE in 1 PACKAGE (0220-9000-59) / 75 g in 1 TUBE
- ndc1102209000651 TUBE in 1 PACKAGE (0220-9000-65) / 14 g in 1 TUBE
- ndc1102209000661 TUBE in 1 PACKAGE (0220-9000-66) / 120 g in 1 TUBE
- ndc1102209000841 TUBE in 1 PACKAGE (0220-9000-84) / 45 g in 1 TUBE
- ndc1102209000852 TUBE in 1 PACKAGE (0220-9000-85) / 120 g in 1 TUBE
- ndc1102209000862 TUBE in 1 PACKAGE (0220-9000-86) / 45 g in 1 TUBE
- ndc1102209000945 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"
}Access this data programmatically
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