{
  "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,
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  "results": [
    {
      "product_ndc": "52000-071",
      "generic_name": "Itch Stopping Cream",
      "labeler_name": "Universal Distribution Centre LLC",
      "brand_name": "Extra Strength Itch Stopping",
      "brand_name_suffix": "Itch Stopping",
      "active_ingredients": [
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          "name": "DIPHENHYDRAMINE HYDROCHLORIDE",
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        {
          "name": "ZINC ACETATE",
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      ],
      "finished": true,
      "packaging": [
        {
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          "description": "1 TUBE in 1 CARTON (52000-071-04)  / 35.4 g in 1 TUBE (52000-071-03)",
          "marketing_start_date": "20210121",
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        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
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      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "CREAM",
      "spl_id": "1853be3d-62de-dc6b-e063-6394a90aad99",
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      "application_number": "M016",
      "brand_name_base": "Extra Strength",
      "pharm_class": [
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        "Decreased Copper Ion Absorption [PE]",
        "Histamine H1 Receptor Antagonists [MoA]",
        "Histamine-1 Receptor Antagonist [EPC]"
      ]
    }
  ]
}