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United States · US · US:0220-9084_3054e90d-d3f8-b5f5-e063-6294a90ae056
Arnicare Bruise
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
- ndc1102209084541 TUBE in 1 PACKAGE (0220-9084-54) / 45 g in 1 TUBE
- ndc1102209084591 TUBE in 1 CARTON (0220-9084-59) / 75 g in 1 TUBE
- ndc1102209084661 TUBE in 1 CARTON (0220-9084-66) / 120 g in 1 TUBE
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": "0220-9084_3054e90d-d3f8-b5f5-e063-6294a90ae056",
"productndc": "0220-9084",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ARNICA MONTANA",
"proprietary_name": "Arnicare Bruise",
"active_ingred_unit": "[hp_X]/g",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "ARNICA MONTANA",
"start_marketing_date": "20160201",
"active_numerator_strength": "1"
}Access this data programmatically
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