{
  "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": "71141-185",
      "generic_name": "Sodium Fluoride",
      "labeler_name": "Lidl US, LLC",
      "brand_name": "dentalux ANTI-CAVITY FLUORIDE WHITENING MINT",
      "active_ingredients": [
        {
          "name": "SODIUM FLUORIDE",
          "strength": ".243 g/100g"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "71141-185-10",
          "description": "1 TUBE in 1 BOX (71141-185-10)  / 113 g in 1 TUBE",
          "marketing_start_date": "20240630",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Lidl US, LLC"
        ],
        "rxcui": [
          "891775"
        ],
        "spl_set_id": [
          "37011052-16ef-4ae4-aade-a86f9fa9cdac"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "4056489867692"
        ],
        "unii": [
          "8ZYQ1474W7"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "PASTE, DENTIFRICE",
      "spl_id": "6e4327b9-2172-4b85-a024-f04a166a330d",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "DENTAL"
      ],
      "marketing_start_date": "20240630",
      "product_id": "71141-185_6e4327b9-2172-4b85-a024-f04a166a330d",
      "application_number": "M021",
      "brand_name_base": "dentalux ANTI-CAVITY FLUORIDE WHITENING MINT"
    }
  ]
}