BluDerma
Toxta

Jetema

Toxta

Brand

Jetema

Category

Botulinum Toxin

Origin

Korea

Options

100 unit

Available options

100 unit

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Overview

Toxta is a botulinum toxin type A injectable manufactured by Jetema Co., Ltd. in South Korea and is KFDA-approved for aesthetic use. It is supplied in 100- and 200-unit lyophilised vials and is marketed on a high-purity, low-protein-load positioning intended to reduce immunogenicity risk. It is used for facial wrinkle treatment and muscle-slimming procedures.

How it works

Botulinum toxin type A blocks acetylcholine release at the neuromuscular junction by cleaving the SNAP-25 protein required for synaptic vesicle fusion. This produces temporary, dose-dependent chemodenervation that relaxes the targeted muscle, softening dynamic wrinkles until nerve terminals regenerate over several months.

Indications

  • Glabellar frown lines
  • Forehead lines
  • Crow's feet
  • Masseter / jaw slimming
  • Dynamic facial wrinkles

Key features

  • Manufactured by Jetema (Korea), KFDA-approved
  • 100- and 200-unit vial options
  • Positioned as high-purity, low protein load
  • Lyophilised powder, saline reconstitution
  • Refrigerated storage, ~36-month shelf life

Benefits

  • Established Korean manufacturer with regulatory approval
  • Low protein load positioned to limit resistance risk
  • Suited to higher-dose use on larger muscles (e.g., masseter)
  • Familiar reconstitution and cold-chain handling

Composition

Botulinum toxin type A, 100 or 200 units per lyophilised vial; distributor listings report human serum albumin and sodium chloride excipients. Reconstituted with sterile 0.9% saline before injection.

Usage & handling

Supplied as a lyophilised powder; reconstitute with preservative-free 0.9% sterile saline. Store sealed and refrigerated at 2-8C, with a reported shelf life of up to 36 months from manufacture; use reconstituted solution promptly. For administration by trained medical professionals only.

For medical professionals. Product information is for reference and does not replace the manufacturer's instructions for use. Availability and regulatory status vary by region.