TriDerma Foot Defense

UNIISPL

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

Identification

ManufacturerGenuine Virgin Aloe Corporation

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
1073806440
1 TUBE in 1 CARTON (10738-064-40) / 119 g in 1 TUBE (10738-064-45)

Annotations

UNII (FDA Substance ID)

344S277G0Z

ALLANTOIN

RxCUI 508

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "344S277G0Z",
    "rxcui": "508",
    "inchikey": "POJWUDADGALRAB-UHFFFAOYSA-N",
    "display_name": "ALLANTOIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "1f11fe3f-487b-4e31-8cdd-2d93560c665f": {
      "match": "brand_token",
      "title": "TRIDERMA STUBBORN ECZEMA ITCH RELIEF (STUBBORN E RELIEF) CREAM [GENUINE VIRGIN ALOE CORPORATION]",
      "spl_version": "1",
      "published_date": "2026-02-02"
    }
  },
  "productid": "10738-064_49784015-9dd8-090d-e063-6294a90a88e4",
  "productndc": "10738-064",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLANTOIN",
  "proprietary_name": "TriDerma Foot Defense",
  "active_ingred_unit": "mg/g",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "TriDerma Foot Defense Cream",
  "start_marketing_date": "20250531",
  "active_numerator_strength": "15"
}

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