{
  "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": "2026-06-03",
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      "spl_product_data_elements": [
        "lumicain Aluminium Chloride Hexahydrate WATER ALUMINUM CHLORIDE ALUMINUM CATION"
      ],
      "dosage_and_administration": [
        "FOR TOPICAL APPLICATION ONLY For Granulation Tissue Growth: Allow packing saturated in Lumicain to remain in nail groove for 48 hours; repeat if necessary. If hemmorrhage is profuse, dress wound with gauze saturated with Lumicain and allow to remain for 24 hours or longer."
      ],
      "warnings_and_cautions": [
        "CAUTION: Federal Law restricts sale and use to physician or licensed practitioner."
      ],
      "package_label_principal_display_panel": [
        "premier lumicain TM Topical Hemostatic Solution 60cc For Rapid Control of Minor Hemorrhage Each Gram Contains: Aluminium Chloride............250 mg. In an aqueous base. Enter section text here lbl"
      ],
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      "id": "b725dd26-c793-51a4-e053-2a95a90a573d",
      "effective_time": "20201223",
      "version": "4",
      "openfda": {
        "brand_name": [
          "lumicain"
        ],
        "generic_name": [
          "ALUMINIUM CHLORIDE HEXAHYDRATE"
        ],
        "manufacturer_name": [
          "Medical Products Laboratories, Inc."
        ],
        "product_ndc": [
          "10733-412"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "TOPICAL"
        ],
        "substance_name": [
          "ALUMINUM CHLORIDE"
        ],
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          "486109"
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        "package_ndc": [
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        "unii": [
          "3CYT62D3GA"
        ]
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}