CLINIQUE SPF 50 BROAD SPECTRUM MINERAL SUNSCREEN FLUID FOR FACE

UNIISPL

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

Identification

ManufacturerCLINIQUE LABORATORIES LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4952775201
1 BOTTLE in 1 CARTON (49527-752-01) / 30 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": {
    "44fe7468-001c-f2ee-e063-6394a90ae3b4": {
      "match": "brand_token",
      "title": "CLINIQUE FOR MEN DAILY HYDRATOR BROAD SPECTRUM SPF 35 (AVOBENZONE,HOMOSALATE,OCTISALATE, AND OCTOCRYLENE) CREAM [CLINIQUE LABORATORIES LLC]",
      "spl_version": "1",
      "published_date": "2025-12-04"
    }
  },
  "productid": "49527-752_2a14c059-489f-546b-e063-6294a90a151c",
  "productndc": "49527-752",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "CLINIQUE SPF 50 BROAD SPECTRUM MINERAL SUNSCREEN FLUID FOR FACE",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "TITANIUM DIOXIDE and ZINC OXIDE",
  "start_marketing_date": "20160601",
  "active_numerator_strength": "63; 40"
}

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