EUPHRASIA OFFICINALIS

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerRxhomeo Private Limited d.b.a. Rxhomeo, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
1563101840
100 PELLET in 1 PACKAGE (15631-0184-0)
ndc11
1563101841
200 PELLET in 1 PACKAGE (15631-0184-1)
ndc11
1563101842
400 PELLET in 1 PACKAGE (15631-0184-2)
ndc11
1563101843
750 PELLET in 1 PACKAGE (15631-0184-3)
ndc11
1563101844
2500 PELLET in 1 PACKAGE (15631-0184-4)
ndc11
1563101845
12500 PELLET in 1 PACKAGE (15631-0184-5)
ndc11
1563101846
500 PELLET in 1 PACKAGE (15631-0184-6)
ndc11
1563101847
1000 PELLET in 1 PACKAGE (15631-0184-7)

Annotations

UNII (FDA Substance ID)

C9642I91WL

EUPHRASIA STRICTA

RxCUI 1353885

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "C9642I91WL",
    "rxcui": "1353885",
    "inchikey": null,
    "display_name": "EUPHRASIA STRICTA",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "26a12b4b-5237-4fed-a827-f6385c6de051": {
      "match": "brand_token",
      "title": "EUPHRASIA OFFICINALIS 7117 (EUPHRASIA OFFICINALIS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "15631-0184_cdda036a-8e4c-1a19-e053-2995a90a834a",
  "productndc": "15631-0184",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "EUPHRASIA STRICTA",
  "proprietary_name": "EUPHRASIA OFFICINALIS",
  "active_ingred_unit": "[hp_X]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "EUPHRASIA OFFICINALIS",
  "start_marketing_date": "20151002",
  "active_numerator_strength": "1"
}

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