UNDA 219

UNII

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

Identification

ManufacturerSeroyal USA

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6210611568
1 BOTTLE, GLASS in 1 CARTON (62106-1156-8) / 20 mL in 1 BOTTLE, GLASS

Annotations

UNII (FDA Substance ID)

Q21UUL2105

CRATAEGUS FRUIT

Raw payload (JSON)

{
  "unii": {
    "unii": "Q21UUL2105",
    "rxcui": null,
    "inchikey": null,
    "display_name": "CRATAEGUS FRUIT",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "62106-1156_ed10cda7-03ea-2f5e-e053-2a95a90a0500",
  "productndc": "62106-1156",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CRATAEGUS FRUIT; LACTUCA VIROSA; PASSIFLORA INCARNATA FLOWERING TOP; THYME; VALERIAN",
  "proprietary_name": "UNDA 219",
  "active_ingred_unit": "[hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Crataegus, Lactuca virosa, Passiflora incarnata, Thymus vulgaris, Valeriana officinalis",
  "start_marketing_date": "20160327",
  "active_numerator_strength": "4; 4; 4; 4; 4"
}

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