Active Ingredient
Lidocaine HCl 0.5%
The following Structured Product Label (SPL) was submitted to the FDA by Chain Drug Marketing Association for the product Pain Relieving Gel (NDC 83324-183). 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 HCl 0.5%
External analgesic
for the temporary relief of pain and itching associated with
For external use only
in large quantities, particularly over raw surfaces or blistered areas
avoid contact with the eyes
condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
If swallowed, get medical help or contact a Poison Control Center right away.
water, propylene glycol, glycerin, Aloe barbadensis leaf juice, triethanolamine, isopropyl alcohol, polysorbate 80, carbomer, phenoxyethanol, benzyl alcohol, menthol, disodium EDTA, blue 1, yellow 5
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