{
  "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": "2026-10-23",
    "results": {
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      "marketing_category": "UNAPPROVED HOMEOPATHIC",
      "dosage_form": "LIQUID",
      "spl_id": "ddbf25ea-80d2-5725-e053-2a95a90abacc",
      "product_type": "HUMAN OTC DRUG",
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      "product_id": "62106-1139_ddbf25ea-80d2-5725-e053-2a95a90abacc",
      "brand_name_base": "UNDA 40",
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        "Copper-containing Intrauterine Device [EPC]",
        "Decreased Embryonic Implantation [PE]",
        "Decreased Sperm Motility [PE]",
        "Dietary Proteins [CS]",
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        "Increased Histamine Release [PE]",
        "Inhibit Ovum Fertilization [PE]",
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        "Non-Standardized Plant Allergenic Extract [EPC]",
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}