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United States · US · US:53645-2270_056793ef-b2b7-1254-e063-6394a90abcf3
Ulmus Radix 6X
UNII
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
- ndc11536452270630 mL in 1 BOTTLE (53645-2270-6)
Annotations
UNII (FDA Substance ID)
9C09P3O90J
ULMUS PARVIFOLIA WHOLE
Raw payload (JSON)
{
"unii": {
"unii": "9C09P3O90J",
"rxcui": null,
"inchikey": null,
"display_name": "ULMUS PARVIFOLIA WHOLE",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"productid": "53645-2270_056793ef-b2b7-1254-e063-6394a90abcf3",
"productndc": "53645-2270",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ULMUS PARVIFOLIA WHOLE",
"proprietary_name": "Ulmus Radix 6X",
"active_ingred_unit": "[hp_X]/30mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Ulmus Radix 6X",
"start_marketing_date": "20230914",
"active_numerator_strength": "6"
}Access this data programmatically
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