{
  "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": "2026-10-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "10157-2106",
      "generic_name": "Benzocaine and ZINC CHLORIDE",
      "labeler_name": "Blistex Inc",
      "brand_name": "KANKA SoftBrush",
      "brand_name_suffix": "SoftBrush",
      "active_ingredients": [
        {
          "name": "BENZOCAINE",
          "strength": "20 mg/100g"
        },
        {
          "name": "ZINC CHLORIDE",
          "strength": ".1 g/100g"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "10157-2106-1",
          "description": "1 APPLICATOR in 1 BLISTER PACK (10157-2106-1)  / 2 g in 1 APPLICATOR",
          "marketing_start_date": "20190925",
          "sample": false
        },
        {
          "package_ndc": "10157-2106-2",
          "description": "2 APPLICATOR in 1 BLISTER PACK (10157-2106-2)  / 2 g in 1 APPLICATOR",
          "marketing_start_date": "20190925",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Blistex Inc"
        ],
        "rxcui": [
          "1249105"
        ],
        "spl_set_id": [
          "093f3545-1d8e-48a3-a533-e9c3ae6d740b"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0041388203928"
        ],
        "nui": [
          "N0000185508",
          "N0000175629",
          "N0000184306",
          "M0000728"
        ],
        "pharm_class_epc": [
          "Standardized Chemical Allergen [EPC]"
        ],
        "pharm_class_pe": [
          "Increased Histamine Release [PE]",
          "Cell-mediated Immunity [PE]"
        ],
        "pharm_class_cs": [
          "Allergens [CS]"
        ],
        "unii": [
          "U3RSY48JW5",
          "86Q357L16B"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "GEL",
      "spl_id": "bbba35d9-5dd7-4471-ad62-63061a9128a1",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20190925",
      "product_id": "10157-2106_bbba35d9-5dd7-4471-ad62-63061a9128a1",
      "application_number": "M022",
      "brand_name_base": "KANKA",
      "pharm_class": [
        "Allergens [CS]",
        "Cell-mediated Immunity [PE]",
        "Copper Absorption Inhibitor [EPC]",
        "Decreased Copper Ion Absorption [PE]",
        "Increased Histamine Release [PE]",
        "Standardized Chemical Allergen [EPC]"
      ]
    }
  ]
}