Luminous Defense SPF 50

UNIISPL

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

Identification

ManufacturerLevels 2 Skin

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8416305615
1 BOTTLE, PLASTIC in 1 BOX (84163-056-15) / 30 mL in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)

SOI2LOH54Z

ZINC OXIDE

RxCUI 11423

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "SOI2LOH54Z",
    "rxcui": "11423",
    "inchikey": "RNWHGQJWIACOKP-UHFFFAOYSA-N",
    "display_name": "ZINC OXIDE",
    "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": "84163-056_22e2c298-3029-c3c9-e063-6394a90a673b",
  "productndc": "84163-056",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Luminous Defense SPF 50",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20250101",
  "active_numerator_strength": "120"
}

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