Unda 245

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
6210611638
1 BOTTLE, GLASS in 1 CARTON (62106-1163-8) / 20 mL in 1 BOTTLE, GLASS

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Raw payload (JSON)

{
  "route": "ORAL",
  "productid": "62106-1163_ed123143-3d42-efb9-e053-2995a90a065c",
  "productndc": "62106-1163",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FAGOPYRUM ESCULENTUM; PULSATILLA VULGARIS; RHEUM TANGUTICUM WHOLE; THUJA OCCIDENTALIS LEAFY TWIG; VIBURNUM PRUNIFOLIUM BARK",
  "proprietary_name": "Unda 245",
  "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": "Rheum, Viburnum prunifolium, Thuja occidentalis, Pulsatilla, Fagopyrum esculentum",
  "start_marketing_date": "20150119",
  "active_numerator_strength": "4; 4; 4; 4; 4"
}

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