Luffa operculata

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
0220316741
6 [hp_C] in 1 TUBE (0220-3167-41)

Annotations

UNII (FDA Substance ID)

C4MO6809HU

LUFFA OPERCULATA FRUIT

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "C4MO6809HU",
    "rxcui": null,
    "inchikey": null,
    "display_name": "LUFFA OPERCULATA FRUIT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "7dbb79de-c3f5-4245-884a-a6bd29bb861c": {
      "match": "brand_token",
      "title": "LUFFA (LUFFA, HYDRASTIS CANADENSIS, MERCURIUS SULPH. RUB, ALLIUM CEPA, NATRUM MURITICUM, PHOSPHORUS, EUPATORIUM PERF, STICTA) TABLET, ORALLY DISINTEGRATING [MARCO PHARMA INTERNATIONAL LLC.]",
      "spl_version": "9",
      "published_date": "2026-01-14"
    }
  },
  "productid": "0220-3167_f6003ca2-33ac-d388-e053-2995a90a8332",
  "productndc": "0220-3167",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LUFFA OPERCULATA FRUIT",
  "proprietary_name": "Luffa operculata",
  "active_ingred_unit": "[hp_C]/6[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "LUFFA OPERCULATA FRUIT",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "6"
}

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