Paris Quadrifolia

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
3766223271
200 PELLET in 1 VIAL, GLASS (37662-2327-1)
ndc11
3766223272
500 PELLET in 1 VIAL, GLASS (37662-2327-2)
ndc11
3766223273
3000 PELLET in 1 BOTTLE, GLASS (37662-2327-3)
ndc11
3766223274
10000 PELLET in 1 BOTTLE, GLASS (37662-2327-4)

Annotations

UNII (FDA Substance ID)

PME3ETQ5WQ

PARIS QUADRIFOLIA

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "PME3ETQ5WQ",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PARIS QUADRIFOLIA",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3a9b9234-9a05-b626-e063-6294a90acedb": {
      "match": "brand_token",
      "title": "PARIS QUADRIFOLIA PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-08-20"
    }
  },
  "productid": "37662-2327_f20a451d-1ce3-cc93-e053-2a95a90a5a15",
  "productndc": "37662-2327",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PARIS QUADRIFOLIA",
  "proprietary_name": "Paris Quadrifolia",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Paris Quadrifolia",
  "start_marketing_date": "20230111",
  "active_numerator_strength": "500"
}

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