Unda 1

ATC D08AL

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

Identification

ManufacturerSeroyal USA

CountryUS (United States)

ATC codeD08AL

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6210611008
1 BOTTLE in 1 CARTON (62106-1100-8) / 20 mL in 1 BOTTLE

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Raw payload (JSON)

{
  "route": "ORAL",
  "productid": "62106-1100_ece42ac2-e879-2756-e053-2995a90a55cb",
  "productndc": "62106-1100",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ACHILLEA MILLEFOLIUM; ANGELICA ARCHANGELICA ROOT; ARCTOSTAPHYLOS UVA-URSI LEAF; EQUISETUM ARVENSE TOP; LARIX DECIDUA RESIN; LYCOPODIUM CLAVATUM SPORE; SILVER; VALERIAN",
  "proprietary_name": "Unda 1",
  "active_ingred_unit": "[hp_X]/20mL; [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": "Achillea millefolium",
  "start_marketing_date": "20140701",
  "active_numerator_strength": "4; 4; 4; 4; 5; 4; 12; 4"
}

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