{
  "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": "2026-10-27",
    "results": {
      "skip": 0,
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  "results": [
    {
      "spl_product_data_elements": [
        "Dr. Talbots Ethyl Alcohol GLYCERIN WATER ALCOHOL ALCOHOL AMINOMETHYL PROPANEDIOL CARBOMER 934"
      ],
      "purpose": [
        "Purpose Antiseptic, Hand Sanitizer Purpose"
      ],
      "indications_and_usage": [
        "Use To help reduce bacteria on the skin that could cause disease. Recommended for repeated use."
      ],
      "warnings": [
        "Warnings For external use only. Flammable. Keep away from heat or flame"
      ],
      "when_using": [
        "When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water."
      ],
      "stop_use": [
        "Stop use and ask a doctor if irritation or redness develops, condition persists for more than 72 hours consult a doctor."
      ],
      "keep_out_of_reach_of_children": [
        "Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away."
      ],
      "dosage_and_administration": [
        "Directions Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision."
      ],
      "storage_and_handling": [
        "Other information Store at normal room temperature May discolor certain fabrics May be harmful to wood finishes and plastics"
      ],
      "inactive_ingredient": [
        "Inactive ingredients aqua, glycerin, carbomer, aminomethyl propanol"
      ],
      "active_ingredient": [
        "Ethyl Alcohol 75%"
      ],
      "package_label_principal_display_panel": [
        "Package Label - Principal Display Panel Principal Display Panel Principal Display Panel Principal Display Panel Principal Display Panel"
      ],
      "set_id": "a6a94205-a9ff-7709-e053-2995a90a066b",
      "id": "2b380620-3e8e-77b0-e063-6394a90a9442",
      "effective_time": "20250108",
      "version": "4",
      "openfda": {
        "application_number": [
          "M014"
        ],
        "brand_name": [
          "Dr. Talbots"
        ],
        "generic_name": [
          "ETHYL ALCOHOL"
        ],
        "manufacturer_name": [
          "Talbots Pharmaceuticals Family Products, LLC."
        ],
        "product_ndc": [
          "70797-160"
        ],
        "product_type": [
          "HUMAN OTC DRUG"
        ],
        "route": [
          "TOPICAL"
        ],
        "substance_name": [
          "ALCOHOL"
        ],
        "rxcui": [
          "1305100"
        ],
        "spl_id": [
          "2b380620-3e8e-77b0-e063-6394a90a9442"
        ],
        "spl_set_id": [
          "a6a94205-a9ff-7709-e053-2995a90a066b"
        ],
        "package_ndc": [
          "70797-160-01",
          "70797-160-02",
          "70797-160-03",
          "70797-160-04"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "3K9958V90M"
        ]
      }
    }
  ]
}