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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
- ndc1102994145001 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"
}Access this data programmatically
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