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United States · US · US:0299-4145_e5783b8b-718a-4b93-8354-029a6b051586

Cetaphil Sun Tinted Face SPF 40

UNIISPL

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

Identification

ManufacturerGalderma Laboratories, L.P.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0299414500
    1 TUBE in 1 CARTON (0299-4145-00) / 50 mL in 1 TUBE

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": {
    "45d101be-2b88-4759-9ccc-556f5ec0553d": {
      "match": "brand_token",
      "title": "CETAPHIL REDNESS RELIEVING DAILY FACIAL MOISTURIZER WITH SUNSCREEN SPF 40 (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [GALDERMA LABORATORIES, L.P.]",
      "spl_version": "4",
      "published_date": "2025-12-19"
    }
  },
  "productid": "0299-4145_e5783b8b-718a-4b93-8354-029a6b051586",
  "productndc": "0299-4145",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "Cetaphil Sun Tinted Face SPF 40",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "titanium dioxide, zinc oxide",
  "start_marketing_date": "20241031",
  "active_numerator_strength": "101; 78"
}

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