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United States · US · US:63127-101_3a740766-e09f-b447-e063-6394a90a6c46
La Defense Broad Spectrum SPF 30 Mineral Sunscreen
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLuzern Laboratories, Inc
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1163127101011 TUBE in 1 CARTON (63127-101-01) / 60 mL in 1 TUBE
- ndc1163127101023 mL in 1 TUBE (63127-101-02)
- ndc116312710103240 mL in 1 BOTTLE (63127-101-03)
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": "63127-101_3a740766-e09f-b447-e063-6394a90a6c46",
"productndc": "63127-101",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
"proprietary_name": "La Defense Broad Spectrum SPF 30 Mineral Sunscreen",
"active_ingred_unit": "g/100mL; g/100mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Zinc Oxide, Titanium Dioxide",
"start_marketing_date": "20210510",
"active_numerator_strength": "3.57; 15"
}Access this data programmatically
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