{
  "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": "2026-10-09",
    "results": {
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    {
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      "generic_name": "Lidocaine Hydrochloride",
      "labeler_name": "Quest Products, LLC.",
      "brand_name": "Alocane Emergency Burn",
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        {
          "name": "LIDOCAINE HYDROCHLORIDE",
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          "description": "1 TUBE in 1 CARTON (68229-201-02)  / 110 mL in 1 TUBE (68229-201-01)",
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          "description": "24 PACKET in 1 CARTON (68229-201-05)  / 3.4 mL in 1 PACKET (68229-201-04)",
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      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
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      "spl_id": "262e0e1d-21b6-be5e-e063-6394a90ab0aa",
      "product_type": "HUMAN OTC DRUG",
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      "product_id": "68229-201_262e0e1d-21b6-be5e-e063-6394a90ab0aa",
      "application_number": "M017",
      "brand_name_base": "Alocane Emergency Burn",
      "pharm_class": [
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        "Amides [CS]",
        "Antiarrhythmic [EPC]",
        "Local Anesthesia [PE]"
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}