Agaricus muscarius

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBoiron

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220012441
6 [hp_X] in 1 TUBE (0220-0124-41)

Annotations

UNII (FDA Substance ID)

RQ7YY49K9Q

AMANITA MUSCARIA WHOLE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "RQ7YY49K9Q",
    "rxcui": null,
    "inchikey": null,
    "display_name": "AMANITA MUSCARIA 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": "0220-0124_0191fcf7-abc0-e583-e063-6294a90a7854",
  "productndc": "0220-0124",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AMANITA MUSCARIA WHOLE",
  "proprietary_name": "Agaricus muscarius",
  "active_ingred_unit": "[hp_X]/6[hp_X]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "AMANITA MUSCARIA WHOLE",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "6"
}

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