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 · 3

ndc11
4996789901
1 BOTTLE, PLASTIC in 1 CARTON (49967-899-01) / 50 mL in 1 BOTTLE, PLASTIC
ndc11
4996789902
1 TUBE in 1 CARTON (49967-899-02) / 3 mL in 1 TUBE
ndc11
4996789903
1 BOTTLE in 1 CARTON (49967-899-03) / 125 mL in 1 BOTTLE

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": "49967-899_2af1e670-d87a-423c-a0dc-9aac07b4166a",
  "productndc": "49967-899",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE",
  "proprietary_name": "La Roche Posay Laboratoire Dermatologique",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium Dioxide",
  "start_marketing_date": "20120601",
  "active_numerator_strength": "110"
}

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