Dermal Fillers
REVOLAX references stocked by ALLPARA for professional use, sourced direct and certified on every shipment.
CE Marked
SKU 11071
·
GTIN 8809427070175
Revolax Fine Lidocaine
In stock
Volume
1 x 1,1 mL
Laboratory
Across Co., Ltd
Origin
South Korea
Indication
Superficial line and delicate facial correction
Treatment areas
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Revolax Fine Lidocaine is a monophasic, cross-linked hyaluronic acid dermal filler by REVOLAX, designed for superficial lines and delicate facial corrections. As the thinnest and most lightweight filler in the REVOLAX range, Revolax Fine with lidocaine is intended for superficial dermal placement to smooth fine lines, crow's feet, glabellar lines, forehead lines and neck wrinkles. The product contains 24 mg/mL of hyaluronic acid with 0.3% lidocaine (3 mg/mL) and is intended strictly for professional use.
Key Benefits of Revolax Fine Lidocaine
- The most lightweight filler in the REVOLAX range, for superficial lines and delicate correction
- Monophasic cross-linked hyaluronic acid at 24 mg/mL, cross-linked with BDDE
- Contains lidocaine hydrochloride 3 mg/mL, 0.3%, giving an analgesic effect during treatment
- Regular, dense monophasic lattice that gives a consistent extrusion force and smooth injection
- High purity hyaluronic acid from bacterial fermentation, of non-animal origin
- Supplied as a 1.1 ml syringe with two ultra thin wall 30G needles
- Duration of 8 to 12 months, with a 24 month shelf life
Indications and Professional Use
Main indications
- Intradermal implantation for volume loss and facial morphological asymmetry
- Superficial lines
- Crow's feet
- Glabellar lines
- Forehead lines
- Neck wrinkles
Professional use
Revolax Fine with Lidocaine is an injectable medical device for administration by trained medical professionals only, and is not for retail sale or self-administration. It is indicated for intradermal implantation and is placed in the superficial dermis, by linear threading or a series of point injections using the needle supplied. Before treatment the patient's suitability and medical history must be assessed, and the patient informed of the indications, contraindications and possible adverse effects. The area to be treated should be disinfected thoroughly and the product injected under sterile conditions; keep the syringe at room temperature for 30 minutes before injection and press the plunger until a small drop is visible at the needle tip. It must not be injected into blood vessels, and it must not be injected into the eye contour, meaning the ocular circle or the eyelids. If the needle blocks, do not increase pressure on the plunger rod; stop and replace the needle. Revolax Fine Lidocaine and Revolax Fine are separate references at different concentrations and volumes, and must not be substituted for one another.
Treatment areas
- Forehead
- Glabellar area
- Crow's feet and the outer eye area
- Neck
Patient profile
For adult patients assessed as suitable by the treating practitioner, typically those seeking correction of superficial lines rather than volume or structural support. It must not be used in women who are pregnant or breastfeeding, in people under 18 years of age, in patients known to be hypersensitive to hyaluronic acid, or in patients who tend to develop hypertrophic scarring. It must not be used in association with laser therapy, chemical peeling or dermabrasion, or in areas presenting cutaneous inflammatory or infectious processes. Because it contains lidocaine, the total dose of lidocaine administered must be taken into account where a dental block or topical lidocaine is used at the same time; high doses above 400 mg can cause acute toxic reactions affecting the central nervous system and cardiac conduction. Lidocaine should be used with caution in patients receiving other local anaesthetics or structurally related agents such as certain antiarrhythmics, since systemic toxic effects may be additive, and in patients with epilepsy, cardiac conduction disorders, severe hepatic impairment or severe renal dysfunction.
How Revolax Fine Lidocaine Works
Revolax Fine Lidocaine works through a monophasic, cross-linked hyaluronic acid gel at 24 mg/mL, combined with 0.3% lidocaine, placed in the superficial dermis. As the lightest-weight gel in the REVOLAX range, this makes it suitable for smoothing superficial lines, crow's feet, glabellar and forehead lines and neck wrinkles.
Why Order From Allpara
Allpara offers genuine, verified REVOLAX products from vetted suppliers, with full batch-traceability and expert support. We serve clinics and aesthetic professionals with CE-certified products, fast EU-wide delivery from our EU warehouse, and competitive trade pricing. Our focus is your patients' safety, satisfaction and results - with dedicated after-sales support for your peace of mind.
Frequently Asked Questions
How does Revolax Fine Lidocaine differ from the plain Revolax Fine?
They differ in more than the anaesthetic. This reference carries hyaluronic acid at 24 mg/mL with lidocaine 0.3% in a 1.1 ml syringe, while the plain Revolax Fine carries 20 mg/mL in a 1 ml syringe. Both are placed in the superficial dermis with 30G needles. Where lidocaine is contraindicated, the plain reference is the one to order.
At what depth is Revolax Fine Lidocaine injected?
In the superficial dermis, the shallowest placement in the REVOLAX range. It must not be injected into the eye contour, meaning the ocular circle or the eyelids.
How long does Revolax Fine Lidocaine last?
Revolax Fine Lidocaine lasts 8 to 12 months, and a clinical investigation confirmed safety and efficacy over a period of 48 weeks. The shelf life of an unopened syringe is 24 months.
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Revolax Fine Lidocaine
In stock
CE Marked
Revolax Fine Lidocaine is a monophasic, cross-linked hyaluronic acid dermal filler by REVOLAX, designed for superficial lines and delicate facial corrections. As the thinnest and most lightweight filler in the REVOLAX range, Revolax Fine with lidocaine is intended for superficial dermal placement to smooth fine lines, crow's feet, glabellar lines, forehead lines and neck wrinkles. The product contains 24 mg/mL of hyaluronic acid with 0.3% lidocaine (3 mg/mL) and is intended strictly for professional use.
Key Benefits of Revolax Fine Lidocaine
- The most lightweight filler in the REVOLAX range, for superficial lines and delicate correction
- Monophasic cross-linked hyaluronic acid at 24 mg/mL, cross-linked with BDDE
- Contains lidocaine hydrochloride 3 mg/mL, 0.3%, giving an analgesic effect during treatment
- Regular, dense monophasic lattice that gives a consistent extrusion force and smooth injection
- High purity hyaluronic acid from bacterial fermentation, of non-animal origin
- Supplied as a 1.1 ml syringe with two ultra thin wall 30G needles
- Duration of 8 to 12 months, with a 24 month shelf life
Indications and Professional Use
Main indications
- Intradermal implantation for volume loss and facial morphological asymmetry
- Superficial lines
- Crow's feet
- Glabellar lines
- Forehead lines
- Neck wrinkles
Professional use
Revolax Fine with Lidocaine is an injectable medical device for administration by trained medical professionals only, and is not for retail sale or self-administration. It is indicated for intradermal implantation and is placed in the superficial dermis, by linear threading or a series of point injections using the needle supplied. Before treatment the patient's suitability and medical history must be assessed, and the patient informed of the indications, contraindications and possible adverse effects. The area to be treated should be disinfected thoroughly and the product injected under sterile conditions; keep the syringe at room temperature for 30 minutes before injection and press the plunger until a small drop is visible at the needle tip. It must not be injected into blood vessels, and it must not be injected into the eye contour, meaning the ocular circle or the eyelids. If the needle blocks, do not increase pressure on the plunger rod; stop and replace the needle. Revolax Fine Lidocaine and Revolax Fine are separate references at different concentrations and volumes, and must not be substituted for one another.
Treatment areas
- Forehead
- Glabellar area
- Crow's feet and the outer eye area
- Neck
Patient profile
For adult patients assessed as suitable by the treating practitioner, typically those seeking correction of superficial lines rather than volume or structural support. It must not be used in women who are pregnant or breastfeeding, in people under 18 years of age, in patients known to be hypersensitive to hyaluronic acid, or in patients who tend to develop hypertrophic scarring. It must not be used in association with laser therapy, chemical peeling or dermabrasion, or in areas presenting cutaneous inflammatory or infectious processes. Because it contains lidocaine, the total dose of lidocaine administered must be taken into account where a dental block or topical lidocaine is used at the same time; high doses above 400 mg can cause acute toxic reactions affecting the central nervous system and cardiac conduction. Lidocaine should be used with caution in patients receiving other local anaesthetics or structurally related agents such as certain antiarrhythmics, since systemic toxic effects may be additive, and in patients with epilepsy, cardiac conduction disorders, severe hepatic impairment or severe renal dysfunction.
How Revolax Fine Lidocaine Works
Revolax Fine Lidocaine works through a monophasic, cross-linked hyaluronic acid gel at 24 mg/mL, combined with 0.3% lidocaine, placed in the superficial dermis. As the lightest-weight gel in the REVOLAX range, this makes it suitable for smoothing superficial lines, crow's feet, glabellar and forehead lines and neck wrinkles.
Why Order From Allpara
Allpara offers genuine, verified REVOLAX products with full batch-traceability, CE-certified stock, fast EU-wide delivery and expert after-sales support.
Frequently Asked Questions
How does Revolax Fine Lidocaine differ from the plain Revolax Fine?
They differ in more than the anaesthetic. This reference carries hyaluronic acid at 24 mg/mL with lidocaine 0.3% in a 1.1 ml syringe, while the plain Revolax Fine carries 20 mg/mL in a 1 ml syringe. Both are placed in the superficial dermis with 30G needles. Where lidocaine is contraindicated, the plain reference is the one to order.
At what depth is Revolax Fine Lidocaine injected?
In the superficial dermis, the shallowest placement in the REVOLAX range. It must not be injected into the eye contour, meaning the ocular circle or the eyelids.
How long does Revolax Fine Lidocaine last?
Revolax Fine Lidocaine lasts 8 to 12 months, and a clinical investigation confirmed safety and efficacy over a period of 48 weeks. The shelf life of an unopened syringe is 24 months.
More from Across
View laboratory →* Professional-use product. Packaging may vary by batch or market. Refer to the supplied IFU for full directions and contraindications.