{
  "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": "2026-10-09",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "82442-201",
      "generic_name": "Menthol Ice",
      "labeler_name": "Target Corporation Inc.",
      "brand_name": "Severe Throat Drops",
      "active_ingredients": [
        {
          "name": "MENTHOL",
          "strength": "20 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "82442-201-01",
          "description": "45 PASTILLE in 1 BAG (82442-201-01)",
          "marketing_start_date": "20240515",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Target Corporation Inc."
        ],
        "rxcui": [
          "1995300"
        ],
        "spl_set_id": [
          "1876b221-fa60-5269-e063-6394a90a6963"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "L7T10EIP3A"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "PASTILLE",
      "spl_id": "1c6cfa26-4422-62d9-e063-6394a90ad7b9",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20240515",
      "product_id": "82442-201_1c6cfa26-4422-62d9-e063-6394a90ad7b9",
      "application_number": "M012",
      "brand_name_base": "Severe Throat Drops"
    }
  ]
}