{
  "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": "Acetaminophen, Dextromethorphan HBr, Doxylamine succinate",
      "labeler_name": "L.N.K. International, Inc.",
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        },
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        {
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      "packaging": [
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          "description": "355 mL in 1 BOTTLE (50844-252-02)",
          "marketing_start_date": "20190714",
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        {
          "package_ndc": "50844-252-45",
          "description": "177 mL in 1 BOTTLE, PLASTIC (50844-252-45)",
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      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
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        "spl_set_id": [
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          "V9BI9B5YI2"
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      "dosage_form": "SOLUTION",
      "spl_id": "50ceb35f-22ce-4af9-9919-29eb609b0d84",
      "product_type": "HUMAN OTC DRUG",
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      "marketing_start_date": "20190714",
      "product_id": "50844-252_50ceb35f-22ce-4af9-9919-29eb609b0d84",
      "application_number": "M012",
      "brand_name_base": "Cold and Flu Nighttime Relief",
      "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]",
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}