{
  "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": "83866-1762",
      "generic_name": "Zinc Oxide",
      "labeler_name": "The Lotus Global Group, Inc, dba GlobalMed Technologies",
      "brand_name": "Omnilux Mineral Facial Sunscreen",
      "active_ingredients": [
        {
          "name": "ZINC OXIDE",
          "strength": "132 mg/mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "83866-1762-2",
          "description": "1 BOTTLE, PUMP in 1 CARTON (83866-1762-2)  / 50 mL in 1 BOTTLE, PUMP (83866-1762-1)",
          "marketing_start_date": "20240726",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "The Lotus Global Group, Inc, dba GlobalMed Technologies"
        ],
        "spl_set_id": [
          "5710c84b-9d6b-da4d-e063-6394a90a0737"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "SOI2LOH54Z"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "LOTION",
      "spl_id": "5710c809-28e3-5748-e063-6294a90a1f52",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "TOPICAL"
      ],
      "marketing_start_date": "20240726",
      "product_id": "83866-1762_5710c809-28e3-5748-e063-6294a90a1f52",
      "application_number": "M020",
      "brand_name_base": "Omnilux Mineral Facial Sunscreen"
    }
  ]
}