Euphrasia Officinalis

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
3766208321
200 PELLET in 1 VIAL, GLASS (37662-0832-1)
ndc11
3766208322
500 PELLET in 1 VIAL, GLASS (37662-0832-2)
ndc11
3766208323
3000 PELLET in 1 BOTTLE, GLASS (37662-0832-3)
ndc11
3766208324
10000 PELLET in 1 BOTTLE, GLASS (37662-0832-4)

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": "37662-0832_e3a2a1ed-daa2-1323-e053-2a95a90afdc0",
  "productndc": "37662-0832",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "EUPHRASIA STRICTA",
  "proprietary_name": "Euphrasia Officinalis",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Euphrasia Officinalis",
  "start_marketing_date": "20220712",
  "active_numerator_strength": "10"
}

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