{
  "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": "2026-10-28",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "spl_product_data_elements": [
        "Max OUT Benzalkonium Chloride POTASSIUM SORBATE SODIUM CHLORIDE CITRIC ACID MONOHYDRATE SODIUM HYDROXYMETHYLGLYCINATE SODIUM BENZOATE BENZALKONIUM CHLORIDE BENZALKONIUM ALOE VERA LEAF WATER"
      ],
      "active_ingredient": [
        "Wipex MAX OUT! Value Sanitizing Wipes Refill Bag Benzalkonium chloride 0.13%"
      ],
      "keep_out_of_reach_of_children": [
        "Keep out of the reach of children. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Contrl right away."
      ],
      "warnings": [
        "Warnings For external use only. Avoid cntact with the eyes. If in eyes, flush thoroughly with water."
      ],
      "inactive_ingredient": [
        "Inactive Ingredients Sodium benzoate, sodium chloride, citric acid, potassium sorbate, sodium hydroxymethylglycinate, aloe vera leaf, water"
      ],
      "purpose": [
        "Purpose Antiseptic"
      ],
      "stop_use": [
        "Stop Use Stop and ask a doctor if: Irritation or redness developes. Conditions persists for more than 72 hours."
      ],
      "dosage_and_administration": [
        "To Use Sanitize hands or other affected area. Discard in trash after use."
      ],
      "indications_and_usage": [
        "To dispense To begin: Break tab on bucket rim and pull off cover. Open bag inside to expose wipes, then thread center wipe through the lid. Replace bucket cover to maintain moisture."
      ],
      "package_label_principal_display_panel": [
        "Max OUT"
      ],
      "set_id": "475903d2-a0b0-5d29-e063-6394a90a528f",
      "id": "475903d2-a0b1-5d29-e063-6394a90a528f",
      "effective_time": "20260101",
      "version": "1",
      "openfda": {
        "application_number": [
          "M032"
        ],
        "brand_name": [
          "Max OUT"
        ],
        "generic_name": [
          "BENZALKONIUM CHLORIDE"
        ],
        "manufacturer_name": [
          "Unico"
        ],
        "product_ndc": [
          "74680-221"
        ],
        "product_type": [
          "HUMAN OTC DRUG"
        ],
        "route": [
          "TOPICAL"
        ],
        "substance_name": [
          "BENZALKONIUM CHLORIDE"
        ],
        "rxcui": [
          "1038558"
        ],
        "spl_id": [
          "475903d2-a0b1-5d29-e063-6394a90a528f"
        ],
        "spl_set_id": [
          "475903d2-a0b0-5d29-e063-6394a90a528f"
        ],
        "package_ndc": [
          "74680-221-88"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "F5UM2KM3W7"
        ]
      }
    }
  ]
}