Luminous Sunscreen SPF 50

UNIISPL

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

Identification

ManufacturerCLINICAL SKIN LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8424802801
1 BOTTLE in 1 CARTON (84248-028-01) / 50 CREAM in 1 BOTTLE

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": {
    "930bd1de-5a0e-4607-8d3c-b1ca918f890b": {
      "match": "brand_token",
      "title": "LUMINOUS EYE CORRECTOR SPF 41 - DEEP (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [DRMTLGY, LLC]",
      "spl_version": "4",
      "published_date": "2026-05-06"
    }
  },
  "productid": "84248-028_26e2b82c-8d7b-7261-e063-6394a90a7c0d",
  "productndc": "84248-028",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "Luminous Sunscreen SPF 50",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide, Titanium Dioxide",
  "start_marketing_date": "20241202",
  "active_numerator_strength": "1.58; 22.4"
}

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