{
  "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": "49967-929",
      "generic_name": "Titanium dioxide and Zinc oxide",
      "labeler_name": "L'Oreal USA Products Inc",
      "brand_name": "SkinCeuticals Physical Matte UV Defense Broad Spectrum SPF 50 Sunscreen",
      "active_ingredients": [
        {
          "name": "TITANIUM DIOXIDE",
          "strength": "90 mg/mL"
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        {
          "name": "ZINC OXIDE",
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      "packaging": [
        {
          "package_ndc": "49967-929-01",
          "description": "1 TUBE in 1 CARTON (49967-929-01)  / 30 mL in 1 TUBE",
          "marketing_start_date": "20150301",
          "sample": false
        },
        {
          "package_ndc": "49967-929-02",
          "description": "1 TUBE in 1 CARTON (49967-929-02)  / 4 mL in 1 TUBE",
          "marketing_start_date": "20150301",
          "sample": false
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      ],
      "listing_expiration_date": "20261231",
      "openfda": {
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        "is_original_packager": [
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        "unii": [
          "15FIX9V2JP",
          "SOI2LOH54Z"
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      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "LOTION",
      "spl_id": "c5ec6166-1a99-4951-b33f-e68359df408c",
      "product_type": "HUMAN OTC DRUG",
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      "product_id": "49967-929_c5ec6166-1a99-4951-b33f-e68359df408c",
      "application_number": "M020",
      "brand_name_base": "SkinCeuticals Physical Matte UV Defense Broad Spectrum SPF 50 Sunscreen",
      "pharm_class": [
        "Copper Absorption Inhibitor [EPC]",
        "Decreased Copper Ion Absorption [PE]"
      ]
    }
  ]
}