{
  "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,
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    }
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  "results": [
    {
      "spl_product_data_elements": [
        "Hand Sanitizer Hand Sanitizer FD&C BLUE NO. 1 D&C RED NO. 33 TROLAMINE WATER ALCOHOL ALCOHOL PROPYLENE GLYCOL GLYCERIN CARBOMER 940 LAVANDULA X INTERMEDIA FLOWER"
      ],
      "active_ingredient": [
        "Active Ingredient(s) Ethyl Alcohol 70% v/v"
      ],
      "purpose": [
        "Purpose Antimicrobial"
      ],
      "indications_and_usage": [
        "Use Uses hand sanitizer to help reduce bacteria on skin."
      ],
      "warnings": [
        "Warnings For external use only. Flammable. Keep away from heat or flame."
      ],
      "do_not_use": [
        "Do not use Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water."
      ],
      "stop_use": [
        "Stop use and ask a doctor if irritation, excessive redness or rash develops."
      ],
      "keep_out_of_reach_of_children": [
        "Keep out of reach of children. Supervise children under 6 years of age when using this product to avoid swallowing. If swallowed, get medical help or contact a Poison Control Center right away."
      ],
      "dosage_and_administration": [
        "Directions Put a dime sized drop onto hands and rub together briskly until dry."
      ],
      "storage_and_handling": [
        "Other information Store below 110℉(43℃)."
      ],
      "inactive_ingredient": [
        "Inactive ingredients Water, glycerin, propylene glycol, fragrance, carbomer, triethanolamine, red 33, blue 1."
      ],
      "package_label_principal_display_panel": [
        "Package Label - Principal Display Panel 59 mL in 1 BOTTLE NDC: 41366-053-01 59ml label"
      ],
      "set_id": "dceced03-eeb8-fced-e053-2995a90afd5c",
      "id": "4545f66c-07fd-6c11-e063-6394a90a9fc8",
      "effective_time": "20251206",
      "version": "3",
      "openfda": {
        "application_number": [
          "M003"
        ],
        "brand_name": [
          "Hand Sanitizer"
        ],
        "generic_name": [
          "HAND SANITIZER"
        ],
        "manufacturer_name": [
          "Zhejiang Meimi Technology Co., Ltd."
        ],
        "product_ndc": [
          "41366-053"
        ],
        "product_type": [
          "HUMAN OTC DRUG"
        ],
        "route": [
          "EXTRACORPOREAL"
        ],
        "substance_name": [
          "ALCOHOL"
        ],
        "rxcui": [
          "581662"
        ],
        "spl_id": [
          "4545f66c-07fd-6c11-e063-6394a90a9fc8"
        ],
        "spl_set_id": [
          "dceced03-eeb8-fced-e053-2995a90afd5c"
        ],
        "package_ndc": [
          "41366-053-01"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0049696866934"
        ],
        "unii": [
          "3K9958V90M"
        ]
      }
    }
  ]
}