Mineral Sunscreen Dry Touch NT

UNIISPL

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

Identification

ManufacturerCutis Wellness Dermatology And Dermatopathology PLLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8543120250
53 g in 1 BOTTLE, PUMP (85431-202-50)

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": {
    "52462e7e-0c2c-6b64-e063-6394a90a4230": {
      "match": "brand_token",
      "title": "MINERAL SPF 30 MOISTURIZER CREAM [DON&RSQUO;T RUN OUT INC (DBA: PUBLIC GOODS)]",
      "spl_version": "2",
      "published_date": "2026-05-25"
    }
  },
  "productid": "85431-202_458708b4-56b7-8d18-e063-6294a90a8c47",
  "productndc": "85431-202",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "Mineral Sunscreen Dry Touch NT",
  "active_ingred_unit": "mg/g; mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium Dioxide, Zinc Oxide",
  "start_marketing_date": "20221028",
  "active_numerator_strength": "80; 38"
}

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