{
  "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": "2026-10-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "product_ndc": "83054-0001",
      "generic_name": "inde wild SUN DEFENSE GLOW DROPS",
      "labeler_name": "INDE WILD PRIVATE LIMITED",
      "brand_name": "inde wild SUN DEFENSE SPF 50 SUNSCREEN GLOW DROPS BROAD SPECTRUM",
      "active_ingredients": [
        {
          "name": "ZINC OXIDE",
          "strength": "12 g/100g"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "83054-0001-3",
          "description": "1 TUBE in 1 PACKAGE (83054-0001-3)  / 30 g in 1 TUBE",
          "marketing_start_date": "20260108",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "INDE WILD PRIVATE LIMITED"
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        "spl_set_id": [
          "47e57407-2925-09ca-e063-6294a90a49ec"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "SOI2LOH54Z"
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      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "LOTION",
      "spl_id": "47e57407-2926-09ca-e063-6294a90a49ec",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "TOPICAL"
      ],
      "marketing_start_date": "20260108",
      "product_id": "83054-0001_47e57407-2926-09ca-e063-6294a90a49ec",
      "application_number": "M020",
      "brand_name_base": "inde wild SUN DEFENSE SPF 50 SUNSCREEN GLOW DROPS BROAD SPECTRUM",
      "pharm_class": [
        "Copper Absorption Inhibitor [EPC]",
        "Decreased Copper Ion Absorption [PE]"
      ]
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  ]
}