Unda 36

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
6210611358
1 BOTTLE, GLASS in 1 CARTON (62106-1135-8) / 20 mL in 1 BOTTLE, GLASS

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Raw payload (JSON)

{
  "route": "ORAL",
  "productid": "62106-1135_ed10a778-ddc9-c29c-e053-2995a90aa5c3",
  "productndc": "62106-1135",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ACONITUM NAPELLUS; ALUMINUM; CHELIDONIUM MAJUS ROOT; GOLDENSEAL; HAMAMELIS VIRGINIANA BARK; HORSE CHESTNUT; HYPERICUM PERFORATUM",
  "proprietary_name": "Unda 36",
  "active_ingred_unit": "[hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Aconitum napellus, Aesculus hippocastanum, Aluminium metallicum, Chelidonium majus, Hamamelis virginiana, Hydrastis canadensis, Hypericum perforatum",
  "start_marketing_date": "20151214",
  "active_numerator_strength": "4; 12; 4; 4; 4; 4; 4"
}

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