{
  "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": "70797-315",
      "generic_name": "Calendula officinalis, Chamomilla, Echinacea angustifolia, Eupatorium perfoliatum, Hepar sulphuris calcareum, Sulphur, Ferrum phosphoricum, Kali muriaticum",
      "labeler_name": "Talbot's Pharmaceuticals Family Products, LLC.",
      "brand_name": "Dr. Talbots Pain Fever Relief",
      "active_ingredients": [
        {
          "name": "MATRICARIA CHAMOMILLA",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "EUPATORIUM PERFOLIATUM FLOWERING TOP",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "CALENDULA OFFICINALIS FLOWERING TOP",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "ECHINACEA ANGUSTIFOLIA",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "CALCIUM SULFIDE",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "POTASSIUM CHLORIDE",
          "strength": "6 [hp_X]/118mL"
        },
        {
          "name": "FERROSOFERRIC PHOSPHATE",
          "strength": "12 [hp_X]/118mL"
        },
        {
          "name": "COSMOS SULPHUREUS FLOWERING TOP",
          "strength": "12 [hp_X]/118mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "70797-315-01",
          "description": "1 BOTTLE in 1 BOTTLE (70797-315-01)  / 118 mL in 1 BOTTLE (70797-315-04)",
          "marketing_start_date": "20200720",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Talbot's Pharmaceuticals Family Products, LLC."
        ],
        "spl_set_id": [
          "91d50391-f6a7-febf-e053-2995a90a1b02"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0370797300059"
        ],
        "unii": [
          "G0R4UBI2ZZ",
          "1W0775VX6E",
          "18E7415PXQ",
          "VB06AV5US8",
          "1MBW07J51Q",
          "660YQ98I10",
          "91GQH8I5F7",
          "WKB165X336"
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      },
      "marketing_category": "UNAPPROVED HOMEOPATHIC",
      "dosage_form": "LIQUID",
      "spl_id": "cda0f5bd-dc31-4faf-e053-2995a90ad4ae",
      "product_type": "HUMAN OTC DRUG",
      "route": [
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      ],
      "marketing_start_date": "20200720",
      "product_id": "70797-315_cda0f5bd-dc31-4faf-e053-2995a90ad4ae",
      "brand_name_base": "Dr. Talbots Pain Fever 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]"
      ]
    }
  ]
}