{
  "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": "2026-10-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "44911-0595",
      "generic_name": "Carbo Vegetabilis, Cuprum Metallicum, Drosera (Rotundifolia), Hepar Sulphuris Calcareum, Ipecacuanha, Lachesis Mutus, Lobelia Inflata, Phosphorus, Pulsatilla (Pratensis), Rumex Crispus, Spongia Tosta",
      "labeler_name": "Energique, Inc.",
      "brand_name": "Upper Resp HP",
      "active_ingredients": [
        {
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          "strength": "30 [hp_X]/mL"
        },
        {
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        },
        {
          "name": "DROSERA ROTUNDIFOLIA WHOLE",
          "strength": "30 [hp_X]/mL"
        },
        {
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          "strength": "30 [hp_X]/mL"
        },
        {
          "name": "IPECAC",
          "strength": "30 [hp_X]/mL"
        },
        {
          "name": "LACHESIS MUTA VENOM",
          "strength": "30 [hp_X]/mL"
        },
        {
          "name": "LOBELIA INFLATA WHOLE",
          "strength": "30 [hp_X]/mL"
        },
        {
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          "strength": "30 [hp_X]/mL"
        },
        {
          "name": "PULSATILLA PRATENSIS WHOLE",
          "strength": "30 [hp_X]/mL"
        },
        {
          "name": "RUMEX CRISPUS ROOT",
          "strength": "30 [hp_X]/mL"
        },
        {
          "name": "SPONGIA OFFICINALIS SKELETON, ROASTED",
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        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "44911-0595-1",
          "description": "30 mL in 1 BOTTLE, DROPPER (44911-0595-1)",
          "marketing_start_date": "20210104",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
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        ],
        "spl_set_id": [
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        "is_original_packager": [
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          "N0000008924",
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        "pharm_class_cs": [
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        "pharm_class_epc": [
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        "pharm_class_pe": [
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          "Decreased Sperm Motility [PE]",
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        "unii": [
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          "789U1901C5",
          "QR44N9XPJQ",
          "1MBW07J51Q",
          "62I3C8233L",
          "VSW71SS07I",
          "9PP1T3TC5U",
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          "8E272251DI",
          "9N1RM2S62C",
          "1PIP394IID"
        ]
      },
      "marketing_category": "UNAPPROVED HOMEOPATHIC",
      "dosage_form": "LIQUID",
      "spl_id": "95dcbcc9-a898-4bd2-92bc-a8d488664c15",
      "product_type": "HUMAN OTC DRUG",
      "route": [
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      ],
      "marketing_start_date": "20210104",
      "product_id": "44911-0595_95dcbcc9-a898-4bd2-92bc-a8d488664c15",
      "brand_name_base": "Upper Resp HP",
      "pharm_class": [
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        "Copper-containing Intrauterine Device [EPC]",
        "Decreased Embryonic Implantation [PE]",
        "Decreased Sperm Motility [PE]",
        "Inhibit Ovum Fertilization [PE]"
      ]
    }
  ]
}