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United States · US · US:49967-525_f1c47f56-d5f5-4eed-8e62-a2aaa579cd02

La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Daily Tone Correcting Primer 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 · 2

  • ndc11
    4996752501
    1 TUBE in 1 CARTON (49967-525-01) / 40 mL in 1 TUBE
  • ndc11
    4996752502
    2 mL in 1 PACKET (49967-525-02)

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": "49967-525_f1c47f56-d5f5-4eed-8e62-a2aaa579cd02",
  "productndc": "49967-525",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE",
  "proprietary_name": "La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Daily Tone Correcting Primer 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": "20160101",
  "active_numerator_strength": "250"
}

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