{
  "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": "2026-10-15",
    "results": {
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      "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride",
      "labeler_name": "United Natural Foods, Inc. dba UNFI",
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      "brand_name_suffix": "extra strength",
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          "name": "DIPHENHYDRAMINE HYDROCHLORIDE",
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          "package_ndc": "41163-515-01",
          "description": "1 BOTTLE, PLASTIC in 1 CARTON (41163-515-01)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC",
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          "package_ndc": "41163-515-03",
          "description": "1 BOTTLE, PLASTIC in 1 CARTON (41163-515-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC",
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      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
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      "spl_id": "24b11c3b-9c19-ff00-e063-6394a90adbed",
      "product_type": "HUMAN OTC DRUG",
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      "product_id": "41163-515_24b11c3b-9c19-ff00-e063-6394a90adbed",
      "application_number": "M013",
      "brand_name_base": "acetaminophen pm",
      "pharm_class": [
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        "Histamine-1 Receptor Antagonist [EPC]"
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}