Foam Weightless Sunscreen Non-Tinted Drytouch 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
8543121104
113 g in 1 BOTTLE, PUMP (85431-211-04)

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": {
    "335ec22c-6a9a-c4d1-e063-6394a90ac0b0": {
      "match": "brand_token",
      "title": "FOAM WEIGHTLESS SUNSCREEN NON-TINTED DRYTOUCH NT (TITANIUM DIOXIDE, ZINC OXIDE) AEROSOL, FOAM [CUTIS WELLNESS DERMATOLOGY AND DERMATOPATHOLOGY PLLC]",
      "spl_version": "2",
      "published_date": "2025-12-10"
    }
  },
  "productid": "85431-211_45870c56-4bcf-5c3b-e063-6394a90a085c",
  "productndc": "85431-211",
  "dosage_form": "AEROSOL, FOAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "Foam Weightless Sunscreen Non-Tinted Drytouch 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": "20230315",
  "active_numerator_strength": "30; 100"
}

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