Oenanthe Crocata

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
3766225131
200 PELLET in 1 VIAL, GLASS (37662-2513-1)
ndc11
3766225132
500 PELLET in 1 VIAL, GLASS (37662-2513-2)
ndc11
3766225133
3000 PELLET in 1 BOTTLE, GLASS (37662-2513-3)
ndc11
3766225134
10000 PELLET in 1 BOTTLE, GLASS (37662-2513-4)

Annotations

UNII (FDA Substance ID)

6FS6FK5S8N

OENANTHE CROCATA ROOT

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "6FS6FK5S8N",
    "rxcui": null,
    "inchikey": null,
    "display_name": "OENANTHE CROCATA ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "21b47ad9-e476-2317-e063-6394a90acfbf": {
      "match": "brand_token",
      "title": "OENANTHE CROCATA (OENANTHE CROCATA ROOT) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2024-09-10"
    }
  },
  "productid": "37662-2513_f3221c6a-cd18-8609-e053-2995a90a4787",
  "productndc": "37662-2513",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OENANTHE CROCATA ROOT",
  "proprietary_name": "Oenanthe Crocata",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Oenanthe Crocata",
  "start_marketing_date": "20230125",
  "active_numerator_strength": "1"
}

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