{
  "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": "2026-10-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "87170-013",
      "generic_name": "Zinx Oxide",
      "labeler_name": "S&C Hampton Sun LLC",
      "brand_name": "Hampton Sun SPF30 Mineral",
      "active_ingredients": [
        {
          "name": "ZINC OXIDE",
          "strength": "19.24 g/100mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "87170-013-01",
          "description": "94.6 mL in 1 TUBE (87170-013-01)",
          "marketing_start_date": "20251201",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "S&C Hampton Sun LLC"
        ],
        "spl_set_id": [
          "019b0c1a-f9f3-4756-8b24-35bf4dc4aa22"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0184573000282"
        ],
        "unii": [
          "SOI2LOH54Z"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "LOTION",
      "spl_id": "51b551c1-436e-a8ab-e063-6294a90a7434",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "TOPICAL"
      ],
      "marketing_start_date": "20251201",
      "product_id": "87170-013_51b551c1-436e-a8ab-e063-6294a90a7434",
      "application_number": "M020",
      "brand_name_base": "Hampton Sun SPF30 Mineral",
      "pharm_class": [
        "Copper Absorption Inhibitor [EPC]",
        "Decreased Copper Ion Absorption [PE]"
      ]
    }
  ]
}