Active Ingredient
Lidocaine HCl 4%
The following Structured Product Label (SPL) was submitted to the FDA by Chain Drug Marketing Association for the product Qc Lidocaine (NDC 63868-956). 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 4%
Topical analgesic
temporarily relieves pain and itching due to:
minor burns
sunburn
minor cuts
scrapes
insect bites
minor skin irritations
For external use only
Do not use in large quantities, particularly over raw surfaces or blistered areas
When using this product do not get into eyes
condition gets worse
symptoms last for more than 7 days
symptoms clear up and occur again within a few days
If swallowed, get medical help or contact a Poison Control Center right away.
adults and children 2 years and over: apply to affected area not more than 3 to 4 times daily
children under 2 years: ask a doctor
store between 20 °C and 25 °C
acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis (aloe vera) leaf juice, aminomethyl propanol,
C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl methicone, cetearyl alcohol, ceteth-20 phosphate, dicetyl phosphate, dimethicone, edetate disodium, ethylhexylglycerin, glyceryl monostearate, methylparaben, purified water, SD alcohol 40, steareth-21
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