Laurocerasus

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
3766217531
200 PELLET in 1 VIAL, GLASS (37662-1753-1)
ndc11
3766217532
500 PELLET in 1 VIAL, GLASS (37662-1753-2)
ndc11
3766217533
3000 PELLET in 1 BOTTLE, GLASS (37662-1753-3)
ndc11
3766217534
10000 PELLET in 1 BOTTLE, GLASS (37662-1753-4)

Annotations

UNII (FDA Substance ID)

F26P2D4757

PRUNUS LAUROCERASUS LEAF

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "F26P2D4757",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PRUNUS LAUROCERASUS LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3a89ddc1-1da7-809c-e063-6294a90a1d2d": {
      "match": "brand_token",
      "title": "LAUROCERASUS (PRUNUS LAUROCERASUS LEAF) PELLET [BOIRON]",
      "spl_version": "2",
      "published_date": "2025-08-20"
    }
  },
  "productid": "37662-1753_ebcf970f-96ec-f0a7-e053-2995a90a07ad",
  "productndc": "37662-1753",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PRUNUS LAUROCERASUS LEAF",
  "proprietary_name": "Laurocerasus",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Laurocerasus",
  "start_marketing_date": "20221024",
  "active_numerator_strength": "100"
}

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