{
  "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": "2026-10-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 413
    }
  },
  "results": [
    {
      "product_ndc": "11673-410",
      "marketing_end_date": "20261231",
      "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl",
      "labeler_name": "TARGET Corporation",
      "brand_name": "Mucus Relief Severe Cold Daytime Maximum Strength",
      "brand_name_suffix": "Daytime Maximum Strength",
      "active_ingredients": [
        {
          "name": "DEXTROMETHORPHAN HYDROBROMIDE",
          "strength": "20 mg/20mL"
        },
        {
          "name": "ACETAMINOPHEN",
          "strength": "650 mg/20mL"
        },
        {
          "name": "GUAIFENESIN",
          "strength": "400 mg/20mL"
        },
        {
          "name": "PHENYLEPHRINE HYDROCHLORIDE",
          "strength": "10 mg/20mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "11673-410-06",
          "description": "177 mL in 1 BOTTLE, PLASTIC (11673-410-06)",
          "marketing_start_date": "20160831",
          "marketing_end_date": "20261231",
          "sample": false
        }
      ],
      "openfda": {
        "manufacturer_name": [
          "TARGET Corporation"
        ],
        "rxcui": [
          "1116572"
        ],
        "spl_set_id": [
          "5ccaf3b0-096a-4644-9c6e-9f251c167b3c"
        ],
        "is_original_packager": [
          true
        ],
        "nui": [
          "N0000193956",
          "N0000008867",
          "N0000009560"
        ],
        "pharm_class_epc": [
          "Expectorant [EPC]"
        ],
        "pharm_class_pe": [
          "Decreased Respiratory Secretion Viscosity [PE]",
          "Increased Respiratory Secretions [PE]"
        ],
        "unii": [
          "9D2RTI9KYH",
          "362O9ITL9D",
          "495W7451VQ",
          "04JA59TNSJ"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "LIQUID",
      "spl_id": "e16dd32c-b538-4a0b-b44f-f43f2ac1e1ce",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20160831",
      "product_id": "11673-410_e16dd32c-b538-4a0b-b44f-f43f2ac1e1ce",
      "application_number": "M012",
      "brand_name_base": "Mucus Relief Severe Cold",
      "pharm_class": [
        "Adrenergic alpha1-Agonists [MoA]",
        "Decreased Respiratory Secretion Viscosity [PE]",
        "Expectorant [EPC]",
        "Increased Respiratory Secretions [PE]",
        "Sigma-1 Agonist [EPC]",
        "Sigma-1 Receptor Agonists [MoA]",
        "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]",
        "Uncompetitive NMDA Receptor Antagonists [MoA]",
        "alpha-1 Adrenergic Agonist [EPC]"
      ]
    }
  ]
}