{
  "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": "2026-10-21",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "70533-001",
      "generic_name": "ZINC OXIDE",
      "labeler_name": "Harry's, Inc.",
      "brand_name": "Daily Face Broad Spectrum",
      "active_ingredients": [
        {
          "name": "ZINC OXIDE",
          "strength": "66 mg/mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "70533-001-50",
          "description": "1 BOTTLE in 1 CARTON (70533-001-50)  / 50 mL in 1 BOTTLE",
          "marketing_start_date": "20160403",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Harry's, Inc."
        ],
        "spl_set_id": [
          "b05b40a9-f02e-43a3-9546-81e14df86972"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "SOI2LOH54Z"
        ]
      },
      "marketing_category": "OTC MONOGRAPH NOT FINAL",
      "dosage_form": "LOTION",
      "spl_id": "2fab0ad2-7453-53fc-e054-00144ff8d46c",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "TOPICAL"
      ],
      "marketing_start_date": "20160401",
      "product_id": "70533-001_2fab0ad2-7453-53fc-e054-00144ff8d46c",
      "application_number": "part352",
      "brand_name_base": "Daily Face Broad Spectrum",
      "pharm_class": [
        "Copper Absorption Inhibitor [EPC]",
        "Decreased Copper Ion Absorption [PE]"
      ]
    }
  ]
}