BELOTERO® SOFT with Lidocaine

Product Description

BELOTERO® SOFT is an advanced dermal filler formulated with hyaluronic acid and lidocaine. This premium product is designed for aesthetic professionals seeking effective solutions for superficial wrinkle correction. The unique formulation ensures seamless integration with the patient’s tissue, providing natural-looking results. Each package contains one 1ml pre-filled syringe and two 30G 1/2″ needles, ready for immediate clinical application.

BELOTERO® SOFT with Lidocaine Dosage and Administration

Professional aesthetic practitioners should administer BELOTERO® SOFT into the superficial dermis using the provided 30G needle. This dermal filler should be injected using a precise technique to ensure optimal distribution and integration with surrounding tissues. Treatment sessions typically take approximately 30 minutes, with visible improvements immediately noticeable. 

The product is designed for single-use only, and practitioners should discard any unused material. For best results, BELOTERO should be administered by healthcare professionals experienced in advanced dermal filler techniques.

Ingredient Information

The primary component of BELOTERO® SOFT is cross-linked sodium hyaluronate at a concentration of 20.0 mg/ml. This hyaluronic acid is derived from non-animal sources, eliminating the need for allergy testing. The product also contains 3.0 mg/ml of lidocaine hydrochloride to reduce discomfort during administration. 

The unique Cohesive Polydensified Matrix (CPM) technology gives this filler exceptional elasticity and cohesivity, allowing for smooth integration with the patient’s skin. All components meet stringent pharmaceutical standards for safety and efficacy.

Storage Instructions

• Store BELOTERO® SOFT with lidocaine between 2°C and 25°C (36°F-77°F) in the original packaging. 

• Keep the product away from direct sunlight and extreme temperatures. 

• Do not freeze this dermal filler. 

• Check the expiration date printed on the package before administration, as expired products should not be used. 

• The sterility of this filler cannot be guaranteed if the package has been opened or damaged.

BELOTERO® SOFT with Lidocaine Contraindications

• BELOTERO® SOFT should not be administered to patients with known hypersensitivity to any of the formulation’s ingredients, particularly hyaluronic acid or lidocaine

• This dermal filler is contraindicated in pregnant or breastfeeding women

• Avoid using this product in areas with active skin infections or inflammatory conditions

• Patients with a history of severe allergies, especially to local anesthetics, should not receive BELOTERO fillers

• This filler should not be injected into blood vessels, as this may lead to serious complications

BELOTERO® SOFT with Lidocaine Precautions and Warnings

Healthcare professionals should exercise caution when administering BELOTERO® SOFT to patients with bleeding disorders or those taking anticoagulant medications. This dermal filler should not be injected into areas where permanent implants have been placed. Practitioners should be aware of vascular anatomy to avoid inadvertent intravascular injection. BELOTERO products should be used with caution in patients with a history of herpes simplex, as the injection procedure may trigger a recurrence. Inform patients that they should avoid makeup application, excessive sun exposure, and extreme temperatures for at least 12 hours after treatment with this filler.

BELOTERO® SOFT with Lidocaine Manufacturer and Regulatory Information

BELOTERO® SOFT with lidocaine is manufactured by Merz Pharma, a globally recognized leader in aesthetic medicine and dermal fillers. Each filler package includes traceability labels that should be affixed to patient records, as required by regulatory requirements. BELOTERO products have an established safety profile and are used by aesthetic professionals in clinical settings worldwide.