{
  "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": "2026-10-07",
    "results": {
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  "results": [
    {
      "product_ndc": "63730-001",
      "generic_name": "TITANIUM DIOXIDE, ZINC OXIDE",
      "labeler_name": "NATURA BISSE INTERNATIONAL SA",
      "brand_name": "Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40",
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        {
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        {
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      "packaging": [
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          "description": "4 mL in 1 PACKET (63730-001-01)",
          "marketing_start_date": "20210601",
          "sample": true
        },
        {
          "package_ndc": "63730-001-02",
          "description": "1 TUBE in 1 BOX (63730-001-02)  / 10 mL in 1 TUBE",
          "marketing_start_date": "20210601",
          "sample": true
        },
        {
          "package_ndc": "63730-001-03",
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        },
        {
          "package_ndc": "63730-001-04",
          "description": "1 TUBE in 1 BOX (63730-001-04)  / 30 mL in 1 TUBE",
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          "sample": false
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      ],
      "listing_expiration_date": "20261231",
      "openfda": {
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      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "LOTION",
      "spl_id": "08aaf4ce-9b1b-5491-e063-6294a90a8a4e",
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        "Decreased Copper Ion Absorption [PE]"
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}