{
  "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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      "generic_name": "Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl",
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          "description": "354 mL in 1 BOTTLE (11673-828-01)",
          "marketing_start_date": "20240630",
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      "listing_expiration_date": "20261231",
      "openfda": {
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      "dosage_form": "LIQUID",
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      "product_type": "HUMAN OTC DRUG",
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      "product_id": "11673-828_1cf3064d-4dde-63b9-e063-6294a90aa547",
      "application_number": "M012",
      "brand_name_base": "Nighttime severe cold and flu",
      "pharm_class": [
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        "Antihistamine [EPC]",
        "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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}