{
  "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": "58466-109",
      "generic_name": "ZINC OXIDE",
      "labeler_name": "Dermazone LLC",
      "brand_name": "78 x 36 SPF 30 Active",
      "active_ingredients": [
        {
          "name": "ZINC OXIDE",
          "strength": ".2 g/g"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "58466-109-03",
          "description": "1 TUBE in 1 CARTON (58466-109-03)  / 96 g in 1 TUBE",
          "marketing_start_date": "20231001",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Dermazone LLC"
        ],
        "spl_set_id": [
          "96a8aacc-5c2f-410a-8fb4-8b3bc0f81e55"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "SOI2LOH54Z"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "CREAM",
      "spl_id": "1c2b73fd-1c52-4db3-982e-d937c04ceeac",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "TOPICAL"
      ],
      "marketing_start_date": "20231001",
      "product_id": "58466-109_1c2b73fd-1c52-4db3-982e-d937c04ceeac",
      "application_number": "M020",
      "brand_name_base": "78 x 36 SPF 30 Active"
    }
  ]
}