{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "0363-6156",
      "marketing_end_date": "20270301",
      "generic_name": "Acetaminophen, Diphenhydramine HCl, Guaifenesin, Phenylephrine HCl",
      "labeler_name": "Walgreen Company",
      "brand_name": "Sinus Pressure and Pain Daytime Nighttime Maximum Strength",
      "brand_name_suffix": "Daytime Nighttime Maximum Strength",
      "finished": true,
      "packaging": [
        {
          "package_ndc": "0363-6156-10",
          "description": "1 KIT in 1 CARTON (0363-6156-10)  *  12 TABLET, FILM COATED in 1 BLISTER PACK *  8 TABLET, FILM COATED in 1 BLISTER PACK",
          "marketing_start_date": "20180602",
          "marketing_end_date": "20270301",
          "sample": false
        }
      ],
      "openfda": {
        "manufacturer_name": [
          "Walgreen Company"
        ],
        "rxcui": [
          "1233575",
          "1243679",
          "2634398"
        ],
        "spl_set_id": [
          "8647c136-a323-453a-8f57-e66938bbf639"
        ],
        "is_original_packager": [
          true
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "KIT",
      "spl_id": "7272f8b1-53fa-4582-88a9-3e4a09861bdf",
      "product_type": "HUMAN OTC DRUG",
      "marketing_start_date": "20180602",
      "product_id": "0363-6156_7272f8b1-53fa-4582-88a9-3e4a09861bdf",
      "application_number": "M012",
      "brand_name_base": "Sinus Pressure and Pain"
    }
  ]
}