Bruselix Gel LIDOCAINE HCI 3.88% PURETEK CORPORATION FDA Approved 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
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Route
TOPICAL
Package NDC

Drug Facts

Composition & Profile

Strengths
57 g
Treats Conditions
Indications For The Temporary Relief Of Pain

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UNII
V13007Z41A
Packaging

HOW SUPPLIED: Bruselix™ Gel is supplied in a 2 oz. (57 g) tube with CRC cap. (NDC 59088-233-05); Bruselix™ Gel Label

Package Descriptions
  • 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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