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United States · US · US:49967-020_9605c52e-22b0-46c9-a93f-bd502aa6073e
La Roche Posay Laboratoire Dermatologique Anthelios 50 Tinted Mineral Face Broad Spectrum SPF 50 Sunscreen
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerL'Oreal USA Products Inc
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1149967020011 BOTTLE, PLASTIC in 1 CARTON (49967-020-01) / 50 mL in 1 BOTTLE, PLASTIC
- ndc1149967020021 TUBE in 1 CARTON (49967-020-02) / 3 mL in 1 TUBE
- ndc1149967020031 BOTTLE in 1 CARTON (49967-020-03) / 125 mL in 1 BOTTLE
- ndc1149967020041 TUBE in 1 CARTON (49967-020-04) / 5 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": {
"851882ac-56f4-4bf6-b942-6efea10eec3e": {
"match": "brand_token",
"title": "LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE BENZOYL PEROXIDE EFFACLAR BPO (BENZOYL PEROXIDE) CREAM [L’OREAL USA PRODUCTS INC]",
"spl_version": "1",
"published_date": "2026-05-28"
}
},
"productid": "49967-020_9605c52e-22b0-46c9-a93f-bd502aa6073e",
"productndc": "49967-020",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TITANIUM DIOXIDE",
"proprietary_name": "La Roche Posay Laboratoire Dermatologique Anthelios 50 Tinted Mineral Face Broad Spectrum SPF 50 Sunscreen",
"active_ingred_unit": "mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Titanium Dioxide",
"start_marketing_date": "20170130",
"active_numerator_strength": "110"
}Access this data programmatically
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