Label: THE DAVINCI COMPANY- lidocaine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 82951-001-01 - Packager: The Davinci Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 25, 2022
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENTActive Ingredient - Lidocaine ............. 0.5%
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PURPOSELidocaine 0.5% ............. Pain Reliever
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INDICATIONS & USAGETemporary relief of pain and itching due to - - sunburn - minor burn - insect bites - minor cuts - scraps
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WARNINGSWarnings - For external use only - When using this product keep out of eyes - Rinse with warter to remove
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STOP USESop use and ask a doctor - system persist for more than 7 days.
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KEEP OUT OF REACH OF CHILDRENKeep out of reach of children. If product is swallowed, get medical help or contact a poison control center right away.
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DOSAGE & ADMINISTRATIONDirection - Adults and children 2 years and older: aooly to affected area not more that 3-4 times a day - Children under 2 years of age: consult a physician.
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INACTIVE INGREDIENTInactive Ingredients: Aloe Barbadensis Leaf Extract, Carbomer, Diazolidinyl Urea, Disodium EDTA, Glycerin, Isopropyl Alcohol, Menthol, Polysorbate 80, Propylene Glycol, Triethanolamine, Water ...
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INGREDIENTS AND APPEARANCEProduct Information