{
  "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": "75568-045",
      "generic_name": "MENTHOL, UNSPECIFIED FORM",
      "labeler_name": "Planet (Anhui) Pharmaceutical Co., Ltd.",
      "brand_name": "BonicaEaseX 24 Hour Menthol Pain Relieving",
      "active_ingredients": [
        {
          "name": "MENTHOL, UNSPECIFIED FORM",
          "strength": "50 mg/g"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "75568-045-00",
          "description": "3 POUCH in 1 BOX (75568-045-00)  / 5 PATCH in 1 POUCH / 9.1 g in 1 PATCH",
          "marketing_start_date": "20260415",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "Planet (Anhui) Pharmaceutical Co., Ltd."
        ],
        "rxcui": [
          "420222"
        ],
        "spl_set_id": [
          "17fc0cd1-710d-45e6-9513-d7100e3adb42"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "L7T10EIP3A"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "PATCH",
      "spl_id": "4f1baa6b-79da-9d1f-e063-6294a90a7477",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "TOPICAL"
      ],
      "marketing_start_date": "20260415",
      "product_id": "75568-045_4f1baa6b-79da-9d1f-e063-6294a90a7477",
      "application_number": "M017",
      "brand_name_base": "BonicaEaseX 24 Hour Menthol Pain Relieving"
    }
  ]
}