Drug Facts
Composition & Profile
Identifiers & Packaging
HOW SUPPLIED: Bruselix™ Gel is supplied in a 2 oz. (57 g) tube with CRC cap. (NDC 59088-233-05); Bruselix™ Gel Label
- HOW SUPPLIED: Bruselix™ Gel is supplied in a 2 oz. (57 g) tube with CRC cap. (NDC 59088-233-05)
- Bruselix™ Gel Label
Overview
Bruselix™ Gel contains 38.8 mg of Lidocaine HCI per gram in a mild acidic vehicle with Aloe Barbadensis (Aloe Vera) Leaf Juice, Aqua (Purified Water), Arnica Montana (Arnica) Flower Extract, Citric Acid, Ethylhexylglycerin, Glycerin, Hydroxyethylcellulose, PEG-4, Phenoxyethanol, Potassium Sorbate, Propylene Glycol, Sodium Benzoate. Lidocaine HCl is chemically designated as acetamide, 2-(diethylamino)-N-(2,6 dimethylphenyl), and has the following structure: Label
Indications & Usage
INDICATIONS: For the temporary relief of pain.
Dosage & Administration
DOSAGE: Apply a thin film to the affected area two or three times daily or as directed by a licensed healthcare practitioner.
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
KEEP THIS AND ALL MEDICATIONS OUT OF THE 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 Panorama City, CA 91402 For questions or information call toll-free: 877-921-7873
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