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United States · US · US:53645-1612_1e8f8326-67f3-d782-e063-6394a90af343
Aconitum 30X
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTrue Botanica, LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11536451612630 mL in 1 BOTTLE (53645-1612-6)
Annotations
UNII (FDA Substance ID)
KPD2N7348X
ACONITUM NAPELLUS ROOT
RxCUI 1330284
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "KPD2N7348X",
"rxcui": "1330284",
"inchikey": null,
"display_name": "ACONITUM NAPELLUS ROOT",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"9d04cb5d-cafa-4a64-bd6e-5724b9ee36ef": {
"match": "brand_token",
"title": "ACONITUM NAPELLUS 7101 (ACONITUM NAPELLUS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
"spl_version": "2",
"published_date": "2026-01-12"
}
},
"productid": "53645-1612_1e8f8326-67f3-d782-e063-6394a90af343",
"productndc": "53645-1612",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACONITUM NAPELLUS ROOT",
"proprietary_name": "Aconitum 30X",
"active_ingred_unit": "[hp_X]/30mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Aconitum 30X",
"start_marketing_date": "20241007",
"active_numerator_strength": "30"
}Access this data programmatically
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