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United States · US · US:69625-019_c41bcab3-9d2a-451f-a678-8fbb37a53161

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

ManufacturerCosmetique Active Production
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    6962501901
    1 BOTTLE, PLASTIC in 1 CARTON (69625-019-01) / 50 mL in 1 BOTTLE, PLASTIC
  • ndc11
    6962501902
    1 TUBE in 1 CARTON (69625-019-02) / 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": "69625-019_c41bcab3-9d2a-451f-a678-8fbb37a53161",
  "productndc": "69625-019",
  "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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