{
  "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": "2026-10-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "83083-002",
      "generic_name": "Activated Mineral Sunscreen Tinted",
      "labeler_name": "Reve Skincare LLC",
      "brand_name": "Activated Mineral Sunscreen Tinted",
      "active_ingredients": [
        {
          "name": "ZINC OXIDE",
          "strength": "142.8 mg/mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "83083-002-50",
          "description": "1 TUBE in 1 CARTON (83083-002-50)  / 50 mL in 1 TUBE",
          "marketing_start_date": "20250325",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Reve Skincare LLC"
        ],
        "spl_set_id": [
          "312a32a7-d253-f10c-e063-6294a90a803a"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0198168599846"
        ],
        "unii": [
          "SOI2LOH54Z"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "CREAM",
      "spl_id": "452053bf-8b70-6550-e063-6294a90a23be",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "TOPICAL"
      ],
      "marketing_start_date": "20250325",
      "product_id": "83083-002_452053bf-8b70-6550-e063-6294a90a23be",
      "application_number": "M020",
      "brand_name_base": "Activated Mineral Sunscreen Tinted"
    }
  ]
}