Unda 42

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
6210611418
1 BOTTLE, GLASS in 1 CARTON (62106-1141-8) / 20 mL in 1 BOTTLE, GLASS

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Raw payload (JSON)

{
  "route": "ORAL",
  "productid": "62106-1141_c7333ab3-5b52-3805-e053-2995a90a48fc",
  "productndc": "62106-1141",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ACONITUM NAPELLUS; ARNICA MONTANA; COPPER; GELSEMIUM SEMPERVIRENS ROOT; GOLD",
  "proprietary_name": "Unda 42",
  "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": "Arnica montana, Aconitum napellus, Gelsemium sempervirens, Aurum metallicum, Cuprum metallicum",
  "start_marketing_date": "20150116",
  "active_numerator_strength": "4; 4; 12; 4; 12"
}

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