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United States · US · US:53645-1621_3bb3a128-253f-5290-e063-6394a90a1797
Agaricus Albus 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
- ndc11536451621630 mL in 1 BOTTLE (53645-1621-6)
Annotations
UNII (FDA Substance ID)
B0FRQ940N7
AGARICUS BISPORUS WHOLE
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "B0FRQ940N7",
"rxcui": null,
"inchikey": null,
"display_name": "AGARICUS BISPORUS WHOLE",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"b6431e0b-6d84-423f-a1be-6701aa848f8d": {
"match": "brand_token",
"title": "AGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]",
"spl_version": "6",
"published_date": "2025-11-24"
}
},
"productid": "53645-1621_3bb3a128-253f-5290-e063-6394a90a1797",
"productndc": "53645-1621",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AGARICUS BISPORUS WHOLE",
"proprietary_name": "Agaricus Albus 30X",
"active_ingred_unit": "[hp_X]/30mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Agaricus Albus 30X",
"start_marketing_date": "20250929",
"active_numerator_strength": "30"
}Access this data programmatically
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