Prunus Spinosa

UNIISPL

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766213701
200 PELLET in 1 VIAL, GLASS (37662-1370-1)
ndc11
3766213702
500 PELLET in 1 VIAL, GLASS (37662-1370-2)
ndc11
3766213703
3000 PELLET in 1 BOTTLE, GLASS (37662-1370-3)
ndc11
3766213704
10000 PELLET in 1 BOTTLE, GLASS (37662-1370-4)

Annotations

UNII (FDA Substance ID)

53Y84VPS2W

PRUNUS SPINOSA FLOWER BUD

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "53Y84VPS2W",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PRUNUS SPINOSA FLOWER BUD",
    "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": "37662-1370_e68a82f1-8448-ef30-e053-2a95a90a9531",
  "productndc": "37662-1370",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PRUNUS SPINOSA FLOWER BUD",
  "proprietary_name": "Prunus Spinosa",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Prunus Spinosa",
  "start_marketing_date": "20220818",
  "active_numerator_strength": "1"
}

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