UNDA 295

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
6210611688
1 BOTTLE, GLASS in 1 CARTON (62106-1168-8) / 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": "62106-1168_ebe194aa-984d-8373-e053-2995a90ae03e",
  "productndc": "62106-1168",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALOE; PULSATILLA VULGARIS; STRYCHNOS NUX-VOMICA SEED",
  "proprietary_name": "UNDA 295",
  "active_ingred_unit": "[hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Pulsatilla, Nux vomica, Aloe socotrina",
  "start_marketing_date": "20150527",
  "active_numerator_strength": "6; 4; 4"
}

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