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United States · US · US:83286-006_4fd2a0b2-4458-423c-8ae4-153bc5fcf58a

LUMINOUS EYE CORRECTOR SPF 41 - DEEP

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerDrmtlgy, LLC
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    8328600601
    1 BOTTLE in 1 CARTON (83286-006-01) / 7 mL 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": "83286-006_4fd2a0b2-4458-423c-8ae4-153bc5fcf58a",
  "productndc": "83286-006",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "LUMINOUS EYE CORRECTOR SPF 41 - DEEP",
  "active_ingred_unit": "g/100mL; g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium dioxide, Zinc oxide",
  "start_marketing_date": "20231222",
  "active_numerator_strength": "10; 12"
}

Access this data programmatically

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