{
  "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": "2026-10-28",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "effective_time": "20111223",
      "inactive_ingredient": [
        "INACTIVE INGREDIENTS WATER, SODIUM LAURETH SULFATE, SODIUM LAURYL SULFATE, COCAMIDE DEA, ZINC CARBONATE, GLYCOL DISTEARATE, FRAGRANCE, DIMETHICONE, CETYL ALCOHOL, POLYQUATERNIUM-10, MAGNESIUM SULFATE, SODIUM BENZOATE, MENTHOL, PEG-7M, MAGNESIUM CARBONATE HYDROXIDE, AMMONIUM LAURETH SULFATE, SEA SALT, FUCUS VESICULOSUS EXTRACT, BENZYL ALCOHOL, SODIUM CHLORIDE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, SODIUM XYLENE SULFONATE, BLUE 1, YELLOW 5"
      ],
      "purpose": [
        "PURPOSE ANTI-DANDRUFF"
      ],
      "keep_out_of_reach_of_children": [
        "KEEP OUT OF REACH OF CHILDREN IF SWALLOWED GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER IMMEDIATELY"
      ],
      "warnings": [
        "WARNINGS FOR EXTERNAL USE ONLY WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER. STOP USE AND ASK A DOCTOR IF CONDITION WORSONS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED KEEP OUT OF REACH OF CHILDREN IF SWALLOWED GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER IMMEDIATELY"
      ],
      "when_using": [
        "WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER."
      ],
      "spl_product_data_elements": [
        "HEB DANDRUFF PYRITHIONE ZINC PYRITHIONE ZINC PYRITHIONE ZINC WATER SODIUM LAURETH SULFATE SODIUM LAURYL SULFATE COCO MONOETHANOLAMIDE ZINC CARBONATE GLYCOL DISTEARATE DIMETHICONE CETYL ALCOHOL POLYQUATERNIUM-10 (400 CPS AT 2%) MAGNESIUM SULFATE, UNSPECIFIED SODIUM BENZOATE MENTHOL POLYETHYLENE GLYCOL 7000 MAGNESIUM CARBONATE HYDROXIDE AMMONIUM LAURETH-3 SULFATE SEA SALT FUCUS VESICULOSUS BENZYL ALCOHOL SODIUM CHLORIDE METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE SODIUM XYLENESULFONATE FD&C BLUE NO. 1 FD&C YELLOW NO. 5"
      ],
      "openfda": {},
      "version": "1",
      "dosage_and_administration": [
        "DIRECTIONS FOR MAXIMUM DANDRUFF CONTROL, USE EVERY TIME YOU SHAMPOO WET HAIR, MASSAGE ONTO SCALP, RINSE, REPEAT IF DESIRED FOR BEST RESULTS USE AT LEAST TWICE A WEEK OR AS DIRECTED BY A DOCTOR"
      ],
      "stop_use": [
        "STOP USE AND ASK A DOCTOR IF CONDITION WORSONS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED"
      ],
      "package_label_principal_display_panel": [
        "LABEL COPY image of the label"
      ],
      "indications_and_usage": [
        "USES HELPS PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF"
      ],
      "set_id": "9e5835e9-28d1-44ef-828d-af5a6c04ea78",
      "id": "530448e2-f128-4609-a3e7-01d4b8fe0edf",
      "active_ingredient": [
        "ACTIVE INGREDIENT PYRITHIONE ZINC 1%"
      ]
    }
  ]
}