Active Ingredient
Lidocaine 0.8% (as Lidocaine HCI)
The following Structured Product Label (SPL) was submitted to the FDA by Wegmans Food Markets Inc for the product Wegmans Aloe After Sun Gel With Lidocaine Hcl External Analgesic (NDC 47124-129). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lidocaine 0.8% (as Lidocaine HCI)
External Analgesic
For the temporary relief of pain and itching associated with sunburn, minor burns, minor cuts, scrapes, insect bites, and minor skin irritations
For External Use Only
in large quantities, particularly over raw surfaces or blistered areas
avoid contact with eyes. If contact occurs, rinse with water to remove.
• condition worsens • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days
If swallowed, seek medical help or contact a Poison Control Center immediately.
• 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.
water, aloe barbadensis leaf juice, SD alcohol 40-B, laureth-23, polysorbate 20, glycerin, allantoin, carbomer, triethanolamine, menthyl lactate, menthol, fragrance, aleurites moluccanus seed extract, carica papaya (papaya) fruit extract, colocasia antiquorum root extract, mangifera indica (mango) fruit extract, passiflora incarnata flower extract, plumeria acutifolia flower extract, psidium guajava fruit extract, tocopheryl acetate (vitamin E acetate), tocopherol, phenoxyethanol, benzyl alcohol, fragrance
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