Prunus spinosa et summ. 30

UNIISPL

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

Identification

ManufacturerUriel Pharmacy, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4895184423
60 mL in 1 BOTTLE, DROPPER (48951-8442-3)

Annotations

UNII (FDA Substance ID)

3MLB4858X7

SLOE

RxCUI 1482548

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "3MLB4858X7",
    "rxcui": "1482548",
    "inchikey": null,
    "display_name": "SLOE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4d7a43b0-f914-e35b-e063-6294a90a0ed3": {
      "match": "brand_token",
      "title": "PRUNUS SPINOSA ET SUMM. 30 LIQUID [URIEL PHARMACY, INC]",
      "spl_version": "1",
      "published_date": "2026-03-23"
    }
  },
  "productid": "48951-8442_4d7a43b0-f915-e35b-e063-6294a90a0ed3",
  "productndc": "48951-8442",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SLOE",
  "proprietary_name": "Prunus spinosa et summ. 30",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Prunus spinosa et summ. 30",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "1"
}

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