{
  "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": "17312-433",
      "generic_name": "Bryonia alba, Hydrastis canadensis, Kali bichromicum, Natrum Muriaticum, Pulsatilla pratensis, Silicea, Stannum metallicum, Thuja occidentalis, Zincum gluconicum",
      "labeler_name": "TRP Company",
      "brand_name": "Mucus and Sinus Mucus and Sinus Symptom Relief",
      "brand_name_suffix": "Mucus and Sinus Symptom Relief",
      "active_ingredients": [
        {
          "name": "BRYONIA ALBA ROOT",
          "strength": "15 [hp_X]/mL"
        },
        {
          "name": "ZINC GLUCONATE",
          "strength": "4 [hp_X]/mL"
        },
        {
          "name": "THUJA OCCIDENTALIS LEAFY TWIG",
          "strength": "12 [hp_X]/mL"
        },
        {
          "name": "TIN",
          "strength": "15 [hp_X]/mL"
        },
        {
          "name": "SILICON DIOXIDE",
          "strength": "15 [hp_X]/mL"
        },
        {
          "name": "PULSATILLA PRATENSIS",
          "strength": "12 [hp_X]/mL"
        },
        {
          "name": "SODIUM CHLORIDE",
          "strength": "6 [hp_X]/mL"
        },
        {
          "name": "POTASSIUM DICHROMATE",
          "strength": "12 [hp_X]/mL"
        },
        {
          "name": "GOLDENSEAL",
          "strength": "12 [hp_X]/mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "17312-433-23",
          "description": "1 BOTTLE, SPRAY in 1 CARTON (17312-433-23)  / 20 mL in 1 BOTTLE, SPRAY",
          "marketing_start_date": "20240806",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "TRP Company"
        ],
        "spl_set_id": [
          "2a42c4a3-9486-9b29-e063-6294a90a7c70"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "T7J046YI2B",
          "U6WSN5SQ1Z",
          "1NT28V9397",
          "387GMG9FH5",
          "ETJ7Z6XBU4",
          "8E272251DI",
          "451W47IQ8X",
          "T4423S18FM",
          "ZW3Z11D0JV"
        ]
      },
      "marketing_category": "UNAPPROVED HOMEOPATHIC",
      "dosage_form": "SPRAY",
      "spl_id": "46064d86-f228-e9e5-e063-6294a90af1ee",
      "product_type": "HUMAN OTC DRUG",
      "route": [
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      ],
      "marketing_start_date": "20240806",
      "product_id": "17312-433_46064d86-f228-e9e5-e063-6294a90af1ee",
      "brand_name_base": "Mucus and Sinus",
      "pharm_class": [
        "Copper Absorption Inhibitor [EPC]",
        "Decreased Copper Ion Absorption [PE]"
      ]
    }
  ]
}