{
  "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": "2026-10-14",
    "results": {
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  "results": [
    {
      "product_ndc": "67777-241",
      "generic_name": "Calamine, Menthol, and Zinc Oxide",
      "labeler_name": "Dynarex Corporation",
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      "packaging": [
        {
          "package_ndc": "67777-241-02",
          "description": "2 BOX in 1 CASE (67777-241-02)  / 144 PACKET in 1 BOX (67777-241-01)  / 3.5 g in 1 PACKET",
          "marketing_start_date": "20260629",
          "sample": false
        },
        {
          "package_ndc": "67777-241-04",
          "description": "36 JAR in 1 CASE (67777-241-04)  / 71 g in 1 JAR (67777-241-03)",
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        },
        {
          "package_ndc": "67777-241-06",
          "description": "24 TUBE in 1 CASE (67777-241-06)  / 113 g in 1 TUBE (67777-241-05)",
          "marketing_start_date": "20260629",
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      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
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      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "OINTMENT",
      "spl_id": "54f12005-acff-4821-e063-6394a90ac304",
      "product_type": "HUMAN OTC DRUG",
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      "product_id": "67777-241_54f12005-acff-4821-e063-6394a90ac304",
      "application_number": "M015",
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