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United States · US · US:53645-2250_05519041-c819-db46-e063-6394a90acd25
Betula Radix 6X
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
- ndc11536452250630 mL in 1 BOTTLE (53645-2250-6)
Annotations
UNII (FDA Substance ID)
SL7A75J492
BETULA PAPYRIFERA WHOLE
RxCUI 1742507
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "SL7A75J492",
"rxcui": "1742507",
"inchikey": null,
"display_name": "BETULA PAPYRIFERA WHOLE",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"7f436fc5-0983-4ce3-9951-e68e395bcab0": {
"match": "brand_token",
"title": "BETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]",
"spl_version": "4",
"published_date": "2025-06-30"
}
},
"productid": "53645-2250_05519041-c819-db46-e063-6394a90acd25",
"productndc": "53645-2250",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BETULA PAPYRIFERA WHOLE",
"proprietary_name": "Betula Radix 6X",
"active_ingred_unit": "[hp_X]/30mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Betula Radix 6X",
"start_marketing_date": "20230914",
"active_numerator_strength": "6"
}Access this data programmatically
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