{
  "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": "69168-393",
      "generic_name": "Acetaminophen 500 mg and Diphenhydramine HCl 25 mg",
      "labeler_name": "Allegiant Health",
      "brand_name": "Pain Relief PM Extra Strength",
      "brand_name_suffix": "Extra Strength",
      "active_ingredients": [
        {
          "name": "ACETAMINOPHEN",
          "strength": "500 mg/1"
        },
        {
          "name": "DIPHENHYDRAMINE HYDROCHLORIDE",
          "strength": "25 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "69168-393-02",
          "description": "150 TABLET in 1 BOTTLE (69168-393-02)",
          "marketing_start_date": "20141223",
          "sample": false
        },
        {
          "package_ndc": "69168-393-24",
          "description": "1 BOTTLE in 1 CARTON (69168-393-24)  / 24 TABLET in 1 BOTTLE",
          "marketing_start_date": "20141223",
          "sample": false
        },
        {
          "package_ndc": "69168-393-26",
          "description": "1 BOTTLE in 1 CARTON (69168-393-26)  / 20 TABLET in 1 BOTTLE",
          "marketing_start_date": "20211215",
          "sample": false
        },
        {
          "package_ndc": "69168-393-50",
          "description": "1 BOTTLE in 1 CARTON (69168-393-50)  / 50 TABLET in 1 BOTTLE",
          "marketing_start_date": "20141223",
          "sample": false
        },
        {
          "package_ndc": "69168-393-99",
          "description": "365 TABLET in 1 BOTTLE (69168-393-99)",
          "marketing_start_date": "20141223",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
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        ],
        "is_original_packager": [
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        "upc": [
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        ],
        "unii": [
          "362O9ITL9D",
          "TC2D6JAD40"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "TABLET",
      "spl_id": "d525d4d3-adac-40fb-a927-832f7d6a831b",
      "product_type": "HUMAN OTC DRUG",
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      "product_id": "69168-393_d525d4d3-adac-40fb-a927-832f7d6a831b",
      "application_number": "M013",
      "brand_name_base": "Pain Relief PM",
      "pharm_class": [
        "Histamine H1 Receptor Antagonists [MoA]",
        "Histamine-1 Receptor Antagonist [EPC]"
      ]
    }
  ]
}