{
  "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": "70797-314",
      "generic_name": "Antimonium tartaricum, Drosera rotundifolia, Ipecacuanha, Phosphorus, Rumex crispus, Spongia Tosta, Sticta pulmonaria, Kali sulphuricum",
      "labeler_name": "Talbot's Pharmaceuticals Family Products, LLC.",
      "brand_name": "Dr. Talbots Cough Relief",
      "active_ingredients": [
        {
          "name": "PULMONARIA OFFICINALIS WHOLE",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "ANTIMONY TARTRATE ION",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "DROSERA ROTUNDIFOLIA FLOWERING TOP",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "PHOSPHORUS",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "RUMEX CRISPUS ROOT",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "POTASSIUM SULFATE",
          "strength": "6 [hp_X]/118mL"
        },
        {
          "name": "SPONGIA OFFICINALIS SKELETON, ROASTED",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "IPECAC",
          "strength": "12 [hp_X]/118mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "70797-314-01",
          "description": "1 BOTTLE in 1 CARTON (70797-314-01)  / 118 mL in 1 BOTTLE (70797-314-04)",
          "marketing_start_date": "20200720",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Talbot's Pharmaceuticals Family Products, LLC."
        ],
        "spl_set_id": [
          "91d3e4d6-356b-4e7f-e053-2a95a90a5158"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0370797300042"
        ],
        "unii": [
          "483B0A2Y00",
          "CQN5KB2U1M",
          "75O014T1HG",
          "27YLU75U4W",
          "9N1RM2S62C",
          "1K573LC5TV",
          "1PIP394IID",
          "62I3C8233L"
        ]
      },
      "marketing_category": "UNAPPROVED HOMEOPATHIC",
      "dosage_form": "LIQUID",
      "spl_id": "cda0f4dc-f551-a6b7-e053-2a95a90a7745",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20200720",
      "product_id": "70797-314_cda0f4dc-f551-a6b7-e053-2a95a90a7745",
      "brand_name_base": "Dr. Talbots Cough Relief",
      "pharm_class": [
        "Increased Large Intestinal Motility [PE]",
        "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]",
        "Osmotic Activity [MoA]",
        "Osmotic Laxative [EPC]",
        "Potassium Compounds [CS]",
        "Potassium Salt [EPC]"
      ]
    }
  ]
}