Melilotus officinalis

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
0220333541
6 [hp_C] in 1 TUBE (0220-3335-41)

Annotations

UNII (FDA Substance ID)

GM6P02J2DX

MELILOTUS OFFICINALIS TOP

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "GM6P02J2DX",
    "rxcui": null,
    "inchikey": null,
    "display_name": "MELILOTUS OFFICINALIS TOP",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "7d792fea-6c10-0994-e053-2a91aa0a20c1": {
      "match": "brand_token",
      "title": "MELILOTUS OFFICINALIS (MELILOTUS OFFICINALIS TOP) PELLET [BOIRON]",
      "spl_version": "3",
      "published_date": "2023-11-15"
    }
  },
  "productid": "0220-3335_0a1f3256-dc5d-91b7-e063-6394a90a0de4",
  "productndc": "0220-3335",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MELILOTUS OFFICINALIS TOP",
  "proprietary_name": "Melilotus officinalis",
  "active_ingred_unit": "[hp_C]/6[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "MELILOTUS OFFICINALIS TOP",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "6"
}

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