{
  "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": "2026-10-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "0031-2099",
      "generic_name": "dextromethorphan hydrobromide, guaifenesin, chlorpheniramine maleate",
      "labeler_name": "Haleon US Holdings LLC",
      "brand_name": "Robitussin Day and Night Cough Relief Value Pack",
      "brand_name_suffix": "Day and Night Cough Relief Value Pack",
      "finished": true,
      "packaging": [
        {
          "package_ndc": "0031-2099-01",
          "description": "1 KIT in 1 CARTON (0031-2099-01)  *  1 BOTTLE in 1 CARTON (0031-8702-13)  / 118 mL in 1 BOTTLE *  1 BOTTLE in 1 CARTON (0031-8692-13)  / 118 mL in 1 BOTTLE",
          "marketing_start_date": "20200512",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Haleon US Holdings LLC"
        ],
        "rxcui": [
          "1111440",
          "1790650",
          "2362250"
        ],
        "spl_set_id": [
          "4029eccd-5443-4ae2-9232-2a1d922798f8"
        ],
        "is_original_packager": [
          true
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "KIT",
      "spl_id": "413911db-b452-6adf-e063-6394a90ac22b",
      "product_type": "HUMAN OTC DRUG",
      "marketing_start_date": "20200512",
      "product_id": "0031-2099_413911db-b452-6adf-e063-6394a90ac22b",
      "application_number": "M012",
      "brand_name_base": "Robitussin"
    }
  ]
}