{
  "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": "2026-10-09",
    "results": {
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    {
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      "generic_name": "Triple Antibiotic",
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        {
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        },
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      "packaging": [
        {
          "package_ndc": "85248-117-01",
          "description": "20 g in 1 TUBE (85248-117-01)",
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          "sample": false
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      ],
      "listing_expiration_date": "20271231",
      "openfda": {
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        "nui": [
          "N0000175499",
          "M0017217"
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        "pharm_class_epc": [
          "Polymyxin-class Antibacterial [EPC]"
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      "dosage_form": "OINTMENT",
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      "product_type": "HUMAN OTC DRUG",
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      "marketing_start_date": "20260209",
      "product_id": "85248-117_572bc9b6-cdd0-89c8-e063-6394a90adc57",
      "application_number": "M004",
      "brand_name_base": "DERMFREE Triple Antibiotic",
      "pharm_class": [
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        "Aminoglycosides [CS]",
        "Decreased Cell Wall Synthesis & Repair [PE]",
        "Polymyxin-class Antibacterial [EPC]",
        "Polymyxins [CS]"
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}