La Roche Posay Laboratoire Dermatologique

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

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
4996790701
1 BOTTLE, PLASTIC in 1 CARTON (49967-907-01) / 50 mL in 1 BOTTLE, PLASTIC
ndc11
4996790703
1 TUBE in 1 CARTON (49967-907-03) / 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&RSQUO;OREAL USA PRODUCTS INC]",
      "spl_version": "1",
      "published_date": "2026-05-28"
    }
  },
  "productid": "49967-907_93f2cacd-67af-4ad8-9e0a-4de8330f808f",
  "productndc": "49967-907",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "La Roche Posay Laboratoire Dermatologique",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium dioxide and Zinc oxide",
  "start_marketing_date": "20110701",
  "active_numerator_strength": "60; 50"
}

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