UNDA 212

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
6210611558
1 BOTTLE, GLASS in 1 CARTON (62106-1155-8) / 20 mL in 1 BOTTLE, GLASS

Annotations

UNII (FDA Substance ID)

V5VD430YW9

ALOE

RxCUI 91263

Raw payload (JSON)

{
  "unii": {
    "unii": "V5VD430YW9",
    "rxcui": "91263",
    "inchikey": null,
    "display_name": "ALOE",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "62106-1155_c73082d2-60ff-4cbf-e053-2a95a90a8f9b",
  "productndc": "62106-1155",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALOE; GOLDENSEAL; MENYANTHES TRIFOLIATA; VIOLA TRICOLOR",
  "proprietary_name": "UNDA 212",
  "active_ingred_unit": "[hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Menyanthes trifoliata, Viola tricolor, Hydrastis canadensis, Aloe socotrina",
  "start_marketing_date": "20150602",
  "active_numerator_strength": "10; 10; 4; 4"
}

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