Coretox 100U

Coretox 100U is a botulinum toxin Type A injection supplied as a lyophilized white powder in a single 100-unit vial, reconstituted with saline before use. It is formulated as neurotoxin only — the complexing proteins are removed — and is made without human serum albumin (HSA) or animal-derived components. Indicated for the temporary improvement of moderate to severe glabellar lines and other dynamic facial wrinkles, it is for licensed practitioners only.

Two-step preparation: Coretox is a lyophilized powder reconstituted with sterile normal saline immediately before use (a saline diluent is commonly supplied). Prepare aseptically and use the reconstituted solution promptly per the practitioner’s protocol.

What’s in Coretox 100U

Clostridium botulinum toxin type A, 100 units per vial.

Coretox blocks the release of acetylcholine at the neuromuscular junction, temporarily relaxing the targeted muscle to soften dynamic wrinkles. Supplied as a lyophilized white powder, reconstituted with saline before injection.

Complexing proteins removed.

Coretox is composed of the neurotoxin only, with the complexing proteins removed. A formulation carrying fewer accessory proteins is positioned to support tolerability over repeated treatment.

Made without human serum albumin or animal-derived components.

Coretox is produced without human serum albumin (HSA) and without animal-derived components, distinguishing its excipient profile from albumin-stabilized toxins.

What Coretox 100U Treats

Coretox 100U Specifications

Coretox 100U — Frequently Asked Questions

What is Coretox 100U?

A botulinum toxin Type A injection supplied as a lyophilized 100-unit powder, reconstituted with saline. It is formulated as neurotoxin only (complexing proteins removed) and made without human serum albumin or animal-derived components.

What makes Coretox different from other toxins?

Its formulation removes the complexing proteins and uses no human serum albumin (HSA) and no animal-derived components, giving it a distinct excipient profile among Type A toxins.

Is Coretox KFDA approved?

Yes. Coretox is MFDS (KFDA) approved in South Korea.

Is it FDA approved?

No. Coretox is not FDA-approved. It is a Korean botulinum toxin Type A for markets where it is authorized.

Does it need reconstitution?

Yes. It is a lyophilized powder reconstituted with sterile normal saline immediately before use, then used promptly.

What areas is it used for?

Moderate to severe glabellar lines and other dynamic facial areas such as the forehead, crow’s feet and eyebrow muscles.

How is it stored?

At 2–8 °C, protected from light, and never frozen. Confirm the expiry date before use.

Who can administer it?

Licensed, trained healthcare professionals only. It is a prescription medical product, not for self-injection or retail sale.

Related Botulinum Toxin Products

Safety Information

Coretox 100U is a prescription botulinum toxin Type A for licensed healthcare professionals only. Do not use in patients with neuromuscular disorders (e.g. myasthenia gravis), known hypersensitivity to botulinum toxin or excipients, active infection at the injection site, or during pregnancy or breastfeeding. Botulinum toxin units are product-specific and are not interchangeable between brands. Aseptic reconstitution and injection technique are essential. Refer to the manufacturer’s prescribing information and the class-wide safety page before administration. Regulatory status varies by jurisdiction; refer to the latest MFDS notice.