{
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    "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": "2026-10-07",
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      "generic_name": "Acetaminophen 325 mg and Dextromethorphan HBr 10 mg Oral Liquid Day Time Kids",
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      "brand_name": "ONESSIP DAY TIME KIDS COLD AND COUGH PLUS FEVER",
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          "strength": "10 mg/10mL"
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      "packaging": [
        {
          "package_ndc": "87078-331-16",
          "description": "16 POUCH in 1 CARTON (87078-331-16)  / 10 mL in 1 POUCH (87078-331-01)",
          "marketing_start_date": "20260515",
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      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
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          "9D2RTI9KYH",
          "362O9ITL9D"
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      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "LIQUID",
      "spl_id": "51d52ce4-98c5-2b9b-e063-6294a90ade44",
      "product_type": "HUMAN OTC DRUG",
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      "application_number": "M012",
      "brand_name_base": "ONESSIP DAY TIME KIDS COLD AND COUGH PLUS FEVER",
      "pharm_class": [
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        "Sigma-1 Receptor Agonists [MoA]",
        "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]",
        "Uncompetitive NMDA Receptor Antagonists [MoA]"
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}