{
  "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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  "results": [
    {
      "product_ndc": "79481-0149",
      "generic_name": "Acetaminophen, Diphenhydramine hydrochloride",
      "labeler_name": "Meijer, Inc.",
      "brand_name": "meijer EXTRA STRENGTH Pain Relief PM Caplet",
      "active_ingredients": [
        {
          "name": "ACETAMINOPHEN",
          "strength": "500 mg/1"
        },
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          "name": "DIPHENHYDRAMINE HYDROCHLORIDE",
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      "packaging": [
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          "description": "1 BOTTLE in 1 CARTON (79481-0149-1)  / 100 TABLET in 1 BOTTLE",
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          "sample": false
        },
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          "package_ndc": "79481-0149-2",
          "description": "2 BOTTLE in 1 CARTON (79481-0149-2)  / 100 TABLET in 1 BOTTLE",
          "marketing_start_date": "20240627",
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        },
        {
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          "marketing_start_date": "20250217",
          "sample": false
        },
        {
          "package_ndc": "79481-0149-5",
          "description": "1 BOTTLE in 1 CARTON (79481-0149-5)  / 50 TABLET in 1 BOTTLE",
          "marketing_start_date": "20240627",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Meijer, Inc."
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      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "TABLET",
      "spl_id": "01e1af5f-2c74-4f27-9273-7470656e21f7",
      "product_type": "HUMAN OTC DRUG",
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      "application_number": "M012",
      "brand_name_base": "meijer EXTRA STRENGTH Pain Relief PM Caplet",
      "pharm_class": [
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        "Histamine-1 Receptor Antagonist [EPC]"
      ]
    }
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}