Label: SUNBURN RELIEF GEL- lidocaine hcl gel

  • NDC Code(s): 30400-605-01
  • Packager: Jell Pharmaceuticals Pvt. Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 19, 2025

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  • Active ingredient
    Lidocaine HCl 0.5%
  • Purpose
    External analgesic
  • Uses
    for the temporary relief of pain and itching associated with - minor burns - sunburn - minor cuts - scrapes - insect bites - minor skin irritations
  • Warnings
    For external use only
  • When using this product
    avoid contact with the eyes
  • Do not use
    in large quantities, particularly over raw surfaces or blistered areas
  • Stop use and ask a doctor if
    condition worsens, or if symptoms persist for more than 7 days or clean up and occur again within a few days
  • Keep out of reach of children
    If swallowed, get medical help or contact a Poison Control Center right away.
  • Directions
    adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily - children under 2 years of age: ask a doctor
  • Inactive ingredients
    water, propylene glycol, glycerin, Aloe Barbadensis Leaf Juice, sodium hydroxide, isopropyl alcohol, polysorbate 80, carbomer, phenoxyethanol, benzyl alcohol, menthol, disodium EDTA, blue 1 ...
  • Principl display panel
    sunburn relief gel - Pain Relieving Gel - with Aloe Vera and Lidocaine HCl
  • INGREDIENTS AND APPEARANCE
    Product Information
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