{
  "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": "2026-10-23",
    "results": {
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    {
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      "marketing_end_date": "20280331",
      "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, and PHENYLEPHRINE HYDROCHLORIDE",
      "labeler_name": "Wal-Mart Stores Inc",
      "brand_name": "NIGHTTIME SEVERE COLD AND FLU",
      "active_ingredients": [
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          "strength": "325 mg/1"
        },
        {
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        },
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        },
        {
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      "packaging": [
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          "package_ndc": "79903-134-24",
          "description": "2 BLISTER PACK in 1 CARTON (79903-134-24)  / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK",
          "marketing_start_date": "20220804",
          "marketing_end_date": "20280331",
          "sample": false
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      "openfda": {
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      "marketing_category": "OTC MONOGRAPH DRUG",
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      "spl_id": "494dd52b-1fac-85bd-e063-6394a90a44f7",
      "product_type": "HUMAN OTC DRUG",
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      "marketing_start_date": "20220804",
      "product_id": "79903-134_494dd52b-1fac-85bd-e063-6394a90a44f7",
      "application_number": "M012",
      "brand_name_base": "NIGHTTIME SEVERE COLD AND FLU",
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        "Histamine Receptor Antagonists [MoA]",
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        "Sigma-1 Receptor Agonists [MoA]",
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}