Active Ingredient
Lidocaine HCl 4%
The following Structured Product Label (SPL) was submitted to the FDA by Gold Bond Co Llc for the product Gold Bond Maximum Strength Foot Pain Relief (NDC 84714-0427). 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, use, warnings, do not use, when using this product, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lidocaine HCl 4%
Topical anesthetic
Temporarily relieves minor pain
For external use only
ask a health professional before use.
If swallowed, get medical help or contact a Poison Control Center immediately.
adults and children over 12 years:
children under 12 years of age: ask a doctor
acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denat. (15%), aloe barbadensis leaf juice, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl methicone, cetearyl alcohol, ceteth-20 phosphate, dicetyl phosphate, dimethicone, disodium EDTA, ethylhexylglycerin, glyceryl stearate, methylparaben, steareth-21, water
Child resistant packaging. Close cap tightly after use.
* Please review the disclaimer below.