Drug Facts
Composition & Profile
Identifiers & Packaging
HOW SUPPLIED PharmaPureRx ® Lidocaine HCl 4.12% Cream 1 oz. (28.3 g) tube - NDC 59088-594-03 3 oz. (85 g) tube - NDC 59088-371-07; PRINCIPAL DISPLAY PharmaPureRx ® Lidocaine HCl 4.12% Cream - carton image description
- HOW SUPPLIED PharmaPureRx ® Lidocaine HCl 4.12% Cream 1 oz. (28.3 g) tube - NDC 59088-594-03 3 oz. (85 g) tube - NDC 59088-371-07
- PRINCIPAL DISPLAY PharmaPureRx ® Lidocaine HCl 4.12% Cream - carton image description
Overview
Contains lidocaine HCl 4.12% in a mild acidic vehicle. Lidocaine is chemically designated as acetamide, 2-(diethylamino)-N-(2,6-dimethylphenyl), and has the following structure: Ingredients: Each gram of PharmaPureRx ® Lidocaine 4.12% Cream contains Lidocaine HCl USP 4.12%. Inactive Ingredients include: Calcium Acetate, Ceteareth 20, Cetearyl Alcohol, Glycerin, Methylparaben, Mineral Oil, Petrolatum, Propylene Glycol, Propylparaben, Purified Water, Sodium Phosphate Monobasic. image description
Indications & Usage
INDICATIONS For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritation.
Dosage & Administration
Apply a thin film to the affected area two or three times daily or as directed by a physician.
Warnings & Precautions
WARNINGS For external use only. Not for ophthalmic use.
Contraindications
Tuberculous or fungal lesions of skin vaccinia, varicella and acute herpes simplex and in persons who have shown hypersensitivity to any of its components. Lidocaine is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.
Adverse Reactions
During or immediately after treatment, the skin at the site of treatment may develop erythema or edema or may be the locus of abnormal sensation.
Storage & Handling
STORAGE AND HANDLING KEEP THIS AND ALL MEDICATIONS OUT OF REACH OF CHILDREN. Store at 20°-25°C (68°-77°F) [see USP Controlled Room Temperature]. Protect from freezing. Manufactured in the USA by: PureTek Corporation San Fernando, CA 91340 Rev. 37886 04/17
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