Veratrum Album

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
3766213031
80 PELLET in 1 VIAL, GLASS (37662-1303-1)
ndc11
3766213032
200 PELLET in 1 VIAL, GLASS (37662-1303-2)
ndc11
3766213033
1200 PELLET in 1 BOTTLE, GLASS (37662-1303-3)
ndc11
3766213034
4000 PELLET in 1 BOTTLE, GLASS (37662-1303-4)

Annotations

UNII (FDA Substance ID)

QNS6W5US1Z

VERATRUM ALBUM ROOT

RxCUI 285168

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "QNS6W5US1Z",
    "rxcui": "285168",
    "inchikey": null,
    "display_name": "VERATRUM ALBUM ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "63597f2a-22c1-41c2-b461-3517447cc03e": {
      "match": "brand_token",
      "title": "VERATRUM COMBINATION 9250 (VERATRUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-1303_e5fafb25-a010-65ba-e053-2a95a90a4228",
  "productndc": "37662-1303",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "VERATRUM ALBUM ROOT",
  "proprietary_name": "Veratrum Album",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Veratrum Album",
  "start_marketing_date": "20220811",
  "active_numerator_strength": "30"
}

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