{
  "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": "2026-10-13",
    "results": {
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  "results": [
    {
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      "generic_name": "homosalate, octisalate, zinc oxide sunscreen",
      "labeler_name": "Swiss-American CDMO, LLC",
      "brand_name": "Private Label SPF 50 80 min Water Resistant",
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      "finished": true,
      "packaging": [
        {
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          "description": "1000 g in 1 TUBE (60232-0035-1)",
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      ],
      "listing_expiration_date": "20261231",
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      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "CREAM",
      "spl_id": "6a3535ae-574f-48d8-bfc0-5b38f54c93ee",
      "product_type": "HUMAN OTC DRUG",
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      "application_number": "M020",
      "brand_name_base": "Private Label SPF 50 80 min Water Resistant",
      "pharm_class": [
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        "Decreased Copper Ion Absorption [PE]"
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}