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United States · US · US:0220-3462_0a1f75ea-3ab2-9953-e063-6294a90a4323
Millefolium
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBoiron
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1102203462419 [hp_C] in 1 TUBE (0220-3462-41)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "ORAL",
"spl_meta": {
"36eb0cf1-1eed-934b-e063-6394a90aeed5": {
"match": "brand_token",
"title": "MILLEFOLIUM 6X LIQUID [URIEL PHARMACY, INC]",
"spl_version": "1",
"published_date": "2025-06-09"
}
},
"productid": "0220-3462_0a1f75ea-3ab2-9953-e063-6294a90a4323",
"productndc": "0220-3462",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACHILLEA MILLEFOLIUM",
"proprietary_name": "Millefolium",
"active_ingred_unit": "[hp_C]/9[hp_C]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "ACHILLEA MILLEFOLIUM",
"start_marketing_date": "19830303",
"active_numerator_strength": "9"
}Access this data programmatically
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