Label: LIDOZALL PLUS- lidocaine hydrochloride cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 24, 2025

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  • Lidozall Plus
    Rapid-onset topical analgesic - Lidozall Plus should be administered under the supervision of a licensed medical practitioner.
  • Active Ingredients
    Lidocaine HCL 4.0% w/w - Purpose - External analgesic
  • Uses
    For temporary relief of pain and itching due to minor skin irritations.
  • Warnings
    - For external use only. - Avoid contact with eyes.
  • DO NOT USE
    - Do not use in large quantities, particularly over raw surfaces or blistered areas.
  • STOP USE
    - Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Discontinue use.
  • KEEP OUT OF REACH OF CHILDREN
    - Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
  • Directions
    For adults and children two-years or older: Apply 1 packet (2 grams) topically to the affected area(s) up to 4 times daily as needed for pain. Do not use more than 4 packets (8 grams) per ...
  • Inactive Ingredients
    Aqua (Deionized Water), Arnica Montana Floweri Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7 ...
  • Other Information
    Protect this product from excessive heat and direct sun.
  • Product Label
    Packaging for Lidozall Plus is shown below:
  • INGREDIENTS AND APPEARANCE
    Product Information
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