Dermaka Sunscreen SPF 42, Tinted

UNIISPL

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

Identification

ManufacturerDERMAKA SKIN PRODUCTS

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8224061900
5 mL in 1 PACKET (82240-619-00)

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": {
    "9a967cd1-9eec-4255-b14b-ac2e33e4dbf0": {
      "match": "brand_token",
      "title": "DERMAKA SUNSCREEN SPF 42, TINTED (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [DERMAKA SKIN PRODUCTS]",
      "spl_version": "1",
      "published_date": "2025-06-18"
    }
  },
  "productid": "82240-619_37b123bf-b595-e935-e063-6394a90a6dd0",
  "productndc": "82240-619",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "Dermaka Sunscreen SPF 42, Tinted",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "TITANIUM DIOXIDE, ZINC OXIDE",
  "start_marketing_date": "20250603",
  "active_numerator_strength": "60; 77"
}

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