{
  "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",
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      "marketing_end_date": "20261231",
      "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate",
      "labeler_name": "P & L Development, LLC",
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      "brand_name_suffix": "ReadyInCase",
      "active_ingredients": [
        {
          "name": "ACETAMINOPHEN",
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        },
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        },
        {
          "name": "DOXYLAMINE SUCCINATE",
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          "package_ndc": "49580-0343-2",
          "description": "355 mL in 1 BOTTLE, PLASTIC (49580-0343-2)",
          "marketing_start_date": "20141031",
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          "description": "177 mL in 1 BOTTLE, PLASTIC (49580-0343-6)",
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      "pharm_class": [
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        "Histamine Receptor Antagonists [MoA]",
        "Sigma-1 Agonist [EPC]",
        "Sigma-1 Receptor Agonists [MoA]",
        "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]",
        "Uncompetitive NMDA Receptor Antagonists [MoA]"
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}