M Lidopro Cream 500g – Lidocaine 2.5% + Prilocaine 2.5% Topical Numbing Cream

M Lidopro Cream 500g is a Korean topical anesthetic cream formulated with lidocaine 2.5% (25mg/g) and prilocaine 2.5% (25mg/g). This dual-ingredient formulation provides temporary localized anesthesia by reducing the transmission of sensory nerve signals in the skin.

Designed for appropriate topical anesthetic applications, M Lidopro Cream is supplied in a generous 500g container, making it a practical packaging option for professional healthcare environments.

Topical anesthetics containing lidocaine and prilocaine are commonly used in clinical settings where temporary surface anesthesia may be needed before certain medical procedures. M Lidopro Cream should only be used according to its approved product labeling and the guidance of a qualified healthcare professional.

Key Features and Benefits of M Lidopro Cream

1. Dual-Ingredient Topical Anesthetic

M Lidopro Cream combines two established local anesthetic ingredients:

• Lidocaine 2.5%: An amide-type local anesthetic that temporarily blocks nerve signal transmission.

• Prilocaine 2.5%: Another amide-type local anesthetic that contributes to localized anesthesia.

Together, these ingredients provide a combined concentration of 5% local anesthetic agents.

2. Temporary Reduction of Skin Sensation

Lidocaine and prilocaine creams are designed to produce temporary localized numbness, helping reduce skin sensitivity during appropriate medical applications.

The degree of anesthesia depends on factors such as application location, skin condition, exposure duration, and individual patient characteristics.

3. Suitable for Professional Healthcare Environments

M Lidopro Cream can be considered by qualified healthcare professionals when a topical anesthetic is appropriate for an authorized clinical procedure.

Potential professional applications of lidocaine and prilocaine formulations include skin preparation before certain needle-based interventions and selected superficial dermatological procedures, subject to the product's specific approved indications.

4. Large 500g Container

The 500g packaging provides a convenient format for professional inventory management.

This larger container may be suitable for healthcare facilities that regularly use topical anesthetics, provided appropriate storage, dispensing, infection-control, and product-handling practices are maintained.

5. Korean Pharmaceutical Product

M Lidopro Cream is presented as a Korean topical anesthetic product. The packaging identifies Tetrapharm Co., Ltd. as its manufacturer.

Active Ingredients and Composition

M Lidopro Cream contains two active local anesthetic ingredients.

Lidocaine – 25mg/g (2.5%)

Lidocaine is an amide-type local anesthetic widely used in medical practice. It works by blocking voltage-gated sodium channels, preventing sensory nerves from transmitting certain signals.

Prilocaine – 25mg/g (2.5%)

Prilocaine belongs to the same general class of local anesthetics. It also acts on sodium channels in nerve membranes, reducing the conduction of sensory impulses.

Combined Active Ingredient Concentration: 5%

Each gram of cream contains 25mg of lidocaine and 25mg of prilocaine, giving a combined total of 50mg of active local anesthetics per gram.

The complete list of inactive ingredients should be checked against the manufacturer's official product documentation.

How Does M Lidopro Cream Work?

M Lidopro Cream works through the local anesthetic effects of lidocaine and prilocaine.

Nerve cells transmit sensory information using electrical impulses. Sodium channels play an essential role in generating and conducting these impulses.

When local anesthetic molecules reach their target nerve structures in sufficient concentrations, they temporarily inhibit sodium channel activity.

This reduces the ability of sensory nerves to transmit signals, producing localized numbness.

The onset, depth, and duration of anesthesia are not identical for every patient or treatment area.

Factors influencing the anesthetic effect include:

• The condition and thickness of the skin

• The amount of cream applied

• The total surface area treated

• The length of application

• Whether the application is covered

• Individual skin characteristics

• The specific clinical procedure

Application quantities and exposure times must follow the approved product instructions rather than a generalized numbing-cream protocol.

Professional Applications of Lidocaine and Prilocaine Cream

Topical anesthetic formulations containing lidocaine and prilocaine have established medical uses.

Depending on the product's regulatory authorization, these may include:

Needle-Related Medical Procedures

Topical anesthesia may be used to reduce discomfort associated with certain needle insertions or other appropriate minor procedures involving intact skin.

Superficial Dermatological Procedures

Qualified healthcare professionals may use approved topical anesthetic formulations before selected superficial skin procedures where local anesthesia is appropriate.

Clinical Skin Preparation

Topical anesthetics may form part of a broader professional preparation process when clinically indicated.

The availability of a particular indication for a lidocaine and prilocaine formulation does not automatically mean M Lidopro Cream is approved for every such procedure.

Use must always be consistent with M Lidopro Cream's country-specific approved labeling.

How to Use M Lidopro Cream

M Lidopro Cream should be used only according to the manufacturer's official instructions or directions from an appropriately qualified healthcare professional.

Before using the product:

1. Confirm that the intended application is appropriate for the patient's clinical needs.

2. Review any history of allergy to lidocaine, prilocaine, or related local anesthetics.

3. Check the recommended application amount, treatment area, and maximum exposure duration against the approved labeling.

4. Follow appropriate skin preparation and infection-control procedures.

5. Remove the cream as directed before proceeding with the intended treatment.

6. Monitor for unexpected skin reactions or symptoms of systemic adverse effects.

Important: Do not independently increase the amount applied, enlarge the treatment area, extend exposure time, or combine the cream with other local anesthetics without professional assessment.

M Lidopro Cream is a topical product and must not be injected or administered intravenously.

Safety Information and Precautions

Although topical lidocaine and prilocaine are established local anesthetics, inappropriate use can cause serious adverse effects.

Do not use M Lidopro Cream if:

• You have a known allergy to lidocaine, prilocaine, or other amide-type local anesthetics.

• You have a known allergy to another ingredient in the formulation.

• The intended application is not supported by the product's approved instructions or professional medical guidance.

Additional precautions:

• Avoid contact with the eyes.

• Do not apply to damaged, inflamed, or broken skin unless specifically authorized by the product labeling.

• Avoid applying excessive quantities or treating unusually large areas.

• Do not use heating devices to increase anesthetic absorption.

• Do not use on mucous membranes unless specifically permitted by the product's approved indications and supervised appropriately.

• Seek professional advice before use during pregnancy or breastfeeding.

• Pediatric use requires age-appropriate medical assessment and specific dosing guidance.

• Inform healthcare professionals about any other local anesthetic products or relevant medications being used.

Lidocaine and prilocaine absorption can increase with larger treated areas, prolonged exposure, and certain application conditions.

Excessive absorption can cause serious systemic toxicity. Prilocaine-containing products can also cause methemoglobinemia, a condition that reduces the blood's ability to transport oxygen.

Symptoms such as blue or gray discoloration of the skin or lips, difficulty breathing, severe dizziness, unusual weakness, seizures, or changes in consciousness require immediate emergency medical attention.

Possible Side Effects

Temporary local skin reactions may occur following topical anesthetic application.

Possible reactions include:

• Mild redness

• Temporary paleness

• Local swelling

• Burning or tingling sensations

• Itching or irritation

Uncommon but potentially serious reactions may include allergic responses, systemic local anesthetic toxicity, or methemoglobinemia.

Stop use and obtain medical assistance if a serious or unexpected reaction occurs.

Product Specifications

Storage and Handling

Store M Lidopro Cream according to the manufacturer's official instructions.

General handling precautions include:

• Keep the container securely closed when not in use.

• Protect the product from excessive heat and unsuitable storage conditions.

• Keep out of the reach of children.

• Avoid contaminating the contents during dispensing.

• Do not use the product after its expiration date.

• Inspect the packaging and cream before use.

Consult the original packaging or product leaflet for the exact approved storage temperature.

Frequently Asked Questions About M Lidopro Cream

What is M Lidopro Cream used for?

M Lidopro Cream is a topical anesthetic formulation containing lidocaine and prilocaine. Its ingredients temporarily reduce localized skin sensation. The product should only be used for indications permitted by its approved labeling.

What are the active ingredients in M Lidopro Cream?

M Lidopro Cream contains lidocaine 2.5% (25mg/g) and prilocaine 2.5% (25mg/g), providing a combined local anesthetic concentration of 5%.

Is M Lidopro Cream the same as a regular lidocaine cream?

Not exactly. M Lidopro Cream combines lidocaine with prilocaine, whereas a lidocaine-only cream contains a single local anesthetic ingredient. Their formulations, approved uses, and application instructions may differ.

How quickly does M Lidopro Cream start working?

The onset of topical anesthesia varies with the application site, skin characteristics, amount applied, and exposure time. Follow the product's official directions for the intended indication rather than assuming a universal onset time.

How long does the numbing effect last?

The duration of anesthesia varies depending on the application conditions and individual response. The manufacturer's approved product information should be used to determine the expected duration for a particular application.

Can M Lidopro Cream be used before aesthetic procedures?

Some lidocaine and prilocaine topical anesthetics are used in healthcare settings before selected superficial procedures. Whether M Lidopro Cream is appropriate for a specific aesthetic treatment must be established by a qualified healthcare professional and the product's approved labeling.

Can M Lidopro Cream be applied to broken skin?

Do not apply to broken or damaged skin unless the specific indication and method are explicitly supported by the approved product instructions and professional guidance.

Is M Lidopro Cream suitable for home use?

The product should only be used in accordance with its regulatory classification, approved labeling, and the requirements of the country where it is supplied. Professional assessment may be necessary.

Can M Lidopro Cream be used with other numbing products?

Combining local anesthetic products can increase total exposure and the risk of adverse effects. Do not combine them without appropriate healthcare professional guidance.

Where is M Lidopro Cream manufactured?

The packaging identifies Tetrapharm Co., Ltd. and indicates that the product is manufactured in South Korea.

What size is M Lidopro Cream available in?

The product described here is supplied in a 500g container.

Important Medical Disclaimer

M Lidopro Cream contains pharmacologically active local anesthetic ingredients. It is not an ordinary cosmetic moisturizer or general skincare cream.

This product description is provided for educational and product-identification purposes only. It does not replace the manufacturer's official instructions, approved prescribing information, or advice from a licensed healthcare professional.

Indications, restrictions, prescription requirements, and legal availability may vary by country.

Always consult the official product labeling and follow applicable medical and regulatory requirements before use.

All Celmade shipments originate from South Korea. We help the main features of sending products to more than 50 countries all around the world.

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• Processing time: 1-3 business days (excluding weekends & holidays).
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• Bulk orders may require import licenses or regulatory approvals in certain countries.
• For U.S. buyers: Some aesthetic medical products (e.g., Botilinum toxin, Fillers) may require FDA clearance. Customers must check local requirements before purchasing.
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Restricted & High-Risk Shipments

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