{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "85735-203",
      "generic_name": "Titanium Dioxide, Zinc Oxide",
      "labeler_name": "LULUS SPA BOUTIQUE",
      "brand_name": "Clear Path Tinted Facial Sunscreen",
      "active_ingredients": [
        {
          "name": "ZINC OXIDE",
          "strength": "38 mg/g"
        },
        {
          "name": "TITANIUM DIOXIDE",
          "strength": "80 mg/g"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "85735-203-50",
          "description": "53 g in 1 BOTTLE, PUMP (85735-203-50)",
          "marketing_start_date": "20180424",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "LULUS SPA BOUTIQUE"
        ],
        "spl_set_id": [
          "37657755-fa82-88a0-e063-6394a90ade47"
        ],
        "unii": [
          "SOI2LOH54Z",
          "15FIX9V2JP"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "CREAM",
      "spl_id": "45782d26-5b24-6cbe-e063-6294a90a4759",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "TOPICAL"
      ],
      "marketing_start_date": "20180424",
      "product_id": "85735-203_45782d26-5b24-6cbe-e063-6294a90a4759",
      "application_number": "M020",
      "brand_name_base": "Clear Path Tinted Facial Sunscreen"
    }
  ]
}