Derma E Sun Defense Face

UNIISPL

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

Identification

Manufacturerderma e

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5410804191
1 TUBE in 1 BOX (54108-0419-1) / 56 g in 1 TUBE

Annotations

UNII (FDA Substance ID)

15FIX9V2JP

TITANIUM DIOXIDE

RxCUI 38323

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "15FIX9V2JP",
    "rxcui": "38323",
    "inchikey": "SOQBVABWOPYFQZ-UHFFFAOYSA-N",
    "display_name": "TITANIUM DIOXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "ba38a43d-7a8a-4814-ba34-0e99124f5fca": {
      "match": "brand_token",
      "title": "DERMA B EVERYDAY FIT SUNSCREEN SPF 50 (AVOBEZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [NEOPHARM CO., LTD.]",
      "spl_version": "2",
      "published_date": "2026-02-06"
    }
  },
  "productid": "54108-0419_dd9fabd4-2126-49ff-aa1a-1e696ad13c56",
  "productndc": "54108-0419",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "Derma E Sun Defense Face",
  "active_ingred_unit": "mg/g; mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide Titanium Dioxide",
  "start_marketing_date": "20221215",
  "active_numerator_strength": "26.4; 195"
}

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