Helonias Dioica

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
3766215021
200 PELLET in 1 VIAL, GLASS (37662-1502-1)
ndc11
3766215022
500 PELLET in 1 VIAL, GLASS (37662-1502-2)
ndc11
3766215023
3000 PELLET in 1 BOTTLE, GLASS (37662-1502-3)
ndc11
3766215024
10000 PELLET in 1 BOTTLE, GLASS (37662-1502-4)

Annotations

UNII (FDA Substance ID)

DQV54Y5H3U

CHAMAELIRIUM LUTEUM ROOT

RxCUI 1322548

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "DQV54Y5H3U",
    "rxcui": "1322548",
    "inchikey": null,
    "display_name": "CHAMAELIRIUM LUTEUM ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "861f6d82-9bd8-4911-a751-9b93ae2210e9": {
      "match": "brand_token",
      "title": "HELONIAS COMBINATION 9227 (HELONIAS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-1502_e8805448-7be3-46d2-e053-2a95a90ae3f6",
  "productndc": "37662-1502",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CHAMAELIRIUM LUTEUM ROOT",
  "proprietary_name": "Helonias Dioica",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Helonias Dioica",
  "start_marketing_date": "20220913",
  "active_numerator_strength": "500"
}

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