{
  "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": "2026-10-14",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "0135-0449",
      "generic_name": "sodium fluoride",
      "labeler_name": "Haleon US Holdings LLC",
      "brand_name": "SENSODYNE PRONAMEL Intensive Enamel Repair Clean Mint",
      "brand_name_suffix": "Intensive Enamel Repair Clean Mint",
      "active_ingredients": [
        {
          "name": "SODIUM FLUORIDE",
          "strength": ".5 mg/mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "0135-0449-01",
          "description": "500 mL in 1 BOTTLE (0135-0449-01)",
          "marketing_start_date": "20240102",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Haleon US Holdings LLC"
        ],
        "rxcui": [
          "240698"
        ],
        "spl_set_id": [
          "817c0dad-d109-428e-adb5-3354604acc94"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "8ZYQ1474W7"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "LIQUID",
      "spl_id": "0a03a9b2-cbbd-4b73-91db-aea9d3a32264",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20240102",
      "product_id": "0135-0449_0a03a9b2-cbbd-4b73-91db-aea9d3a32264",
      "application_number": "M022",
      "brand_name_base": "SENSODYNE PRONAMEL"
    }
  ]
}