Label: COMFORTOX LIDOCAINE- lidocaine hydrochloride cream
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Contains inactivated NDC Code(s)
NDC Code(s): 54723-998-01 - Packager: Sambria Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 3, 2023
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- Official Label (Printer Friendly)
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Active Ingredient
Lidocaine HCL 4.00% w/w - Purpose - External Analgesic
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Uses
For temporary relief of pain and itching due to minor skin irritation.
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Warnings
For external use only - Avoid contact with eyes - Do not use in large quantities, particularly over raw surfaces or blistered areas
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STOP USEStop use and ask a doctor if • Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Discontinue use.
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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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Directions
For adults and children two-years or older: Apply to affected area not more than 3 or 4 times daily. Children under 2 years of age: consult a physician. Apply in a circular motion for 50 to 60 ...
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Inactive Ingredients
Aqua (Deionized Water), Arnica Montana Flower Extract, C13-14 Isoparaffin, Chrondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexyglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7 ...
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Other Information
Protect this product from excessive heat and direct sun.
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Questions or Comments?
FDA Registered: NDC No. 54723-998-01 - 800-693-9067
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information