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United States Β· US Β· US:63083-7121_592af89d-eef5-4dd2-904e-5e35c5e213c7

Hypericum perforatum

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerProfessional Complementary Health Formulas
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 1

  • ndc11
    6308371211
    29.5 mL in 1 BOTTLE, DROPPER (63083-7121-1)

Annotations

UNII (FDA Substance ID)
XK4IUX8MNB
HYPERICUM PERFORATUM WHOLE
RxCUI 258326
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "XK4IUX8MNB",
    "rxcui": "258326",
    "inchikey": null,
    "display_name": "HYPERICUM PERFORATUM WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "50125b08-99b9-59aa-e063-6394a90ab9d5": {
      "match": "brand_token",
      "title": "HYPERICUM 3X LIQUID [URIEL PHARMACY, INC]",
      "spl_version": "1",
      "published_date": "2026-04-24"
    }
  },
  "productid": "63083-7121_592af89d-eef5-4dd2-904e-5e35c5e213c7",
  "productndc": "63083-7121",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HYPERICUM PERFORATUM WHOLE",
  "proprietary_name": "Hypericum perforatum",
  "active_ingred_unit": "[hp_X]/29.5mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Hypericum perforatum",
  "start_marketing_date": "19840815",
  "active_numerator_strength": "6"
}

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Hypericum perforatum (US) β€” Drug Database