{
  "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": "87150-001",
      "generic_name": "MENTHOL, 0.11%",
      "labeler_name": "BENOVA RX LLC",
      "brand_name": "BENOVA PAIN AND ITCH RELIEF",
      "active_ingredients": [
        {
          "name": "MENTHOL",
          "strength": "1.1 mg/mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "87150-001-03",
          "description": "90 mL in 1 BOTTLE, WITH APPLICATOR (87150-001-03)",
          "marketing_start_date": "20251215",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "BENOVA RX LLC"
        ],
        "rxcui": [
          "2728901"
        ],
        "spl_set_id": [
          "42513ee2-8b40-a9f3-e063-6394a90a9386"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0860008040763"
        ],
        "unii": [
          "L7T10EIP3A"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "LOTION",
      "spl_id": "42513ee2-8b41-a9f3-e063-6394a90a9386",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "TOPICAL"
      ],
      "marketing_start_date": "20251215",
      "product_id": "87150-001_42513ee2-8b41-a9f3-e063-6394a90a9386",
      "application_number": "M017",
      "brand_name_base": "BENOVA PAIN AND ITCH RELIEF"
    }
  ]
}