Hitox® – Botulinum Toxin Type A [South Korea]

Field Name Example Value
Product Name Hitox® – Botulinum Toxin Type A [South Korea]
Product Code TX-SK-100-886611
Product Type Branded Pharmaceutical / Botulinum Toxin
Category Skin Health / Botulinum Toxin
Manufacturer Huons Biopharma (or actual licensed manufacturer – please confirm)
Appearance White lyophilized powder in clear glass vial
Dosage / Units 100 units per vial
Purity N/A (Biological product; potency measured in Units)
Quantity Options 100ui
Storage Store refrigerated at 2–8°C; protect from light and moisture. Do not freeze.
Shelf Life 24 months unopened
Packaging Korean original retail box with Korean-language leaflet and anti-counterfeit seal
Manufacturer Origin South Korea
Use Classification Export Only – Not for domestic distribution or therapeutic use
Tags hitox, botulinum toxin, korean botox, wrinkle treatment, aesthetic injection, BLUEBIOTECH

⚠️This product is labeled for Research Use Only (RUO). Not for human or veterinary therapeutic use.
See RUO Declaration for more info.

Hitox® – Botulinum Toxin Type A | Korean-Made Export-Grade Toxin

Product Overview

Hitox® is a Botulinum Toxin Type A developed and manufactured in South Korea, designed exclusively for export markets. Produced under GMP-compliant pharmaceutical conditions, Hitox® offers stable potency, controlled diffusion, and high batch consistency—making it a cost-effective and dependable option for overseas buyers seeking high-quality botulinum products for non-clinical or investigational purposes.

While not as internationally established as Botox®, Nabota®, or Botulax®, Hitox® has gained attention among global distributors and research procurement agents for its balance of performance and affordability. This version is strictly intended for export and is not approved for therapeutic or cosmetic use.


Key Features & Advantages

  • Made in South Korea
    Manufactured under GMP-certified conditions by a licensed Korean pharmaceutical company.

  • Export-Grade Toxin
    Intended exclusively for international markets; not available in the domestic (Korean) clinical market.

  • Reliable Formulation
    Consistent biological activity and low bacterial protein content to support reproducible non-clinical testing.

  • Competitive Alternative
    Offers cost-effective access to botulinum toxin for global distributors, labs, and institutions with regulatory clearance.

  • Controlled Diffusion & Fast Onset
    Onset of effect typically begins within 2–3 days under experimental conditions, with localized response lasting several weeks.


Product Specifications

  • Product Name: Hitox® – Botulinum Toxin Type A

  • Form: Lyophilized powder

  • Packaging: 100 Units / vial

  • Appearance: White to off-white powder; forms a clear solution upon reconstitution

  • Manufacturer: Korean pharmaceutical manufacturer (name available upon request)

  • Origin: South Korea

  • Storage Conditions: Store at 2°C–8°C; use within 24 hours after reconstitution

  • Classification: For Export Use Only – Not registered for clinical or cosmetic use in the country of origin


Mechanism of Action

Hitox® exerts its biological effect by blocking the release of acetylcholine at the neuromuscular junction. After internalization into the nerve terminal, its light chain cleaves the SNAP-25 protein, disrupting the SNARE complex required for neurotransmitter vesicle fusion. This temporary inhibition results in localized muscle paralysis or relaxation.

This mechanism is widely studied in the context of dynamic wrinkle formation, chronic muscular conditions, facial rebalancing, and neuromodulatory signaling pathways. Hitox® serves as a reference-grade agent for non-clinical settings requiring reproducible neuromuscular blockade.

For foundational research on botulinum toxin action, refer to NIH Open Access Review.


Use Cases in Export Markets

  • Product sampling for market evaluation

  • Non-clinical investigational studies

  • Pre-clinical formulation or toxin comparison projects

  • Sales channels requiring low-cost, export-grade neurotoxin

  • Institutional procurement in countries with local registration pathways


Compliance Statement

This product is manufactured in South Korea and labeled exclusively for overseas export purposes. It is not registered or approved for clinical, cosmetic, or therapeutic use in any domestic market, and must not be used for human or animal injection. All importers, distributors, and end users are responsible for complying with local laws and regulations in their destination country.


Tags / Keywords

Hitox, Korean Botulinum Toxin, Export-Grade Toxin, Botulinum Toxin Type A, Botulinum for Export, SNAP-25 Research, Acetylcholine Blockade, Emerging Botulinum Brand, Botulinum Toxin for Distributor Use, GMP Korean Toxin


External References

Corporate Advantages

High-Purity Standards

Tested for purity and identity. COAs available
for all RUO compounds

Buyer Protection

Protected and discrete fulfillment
available upon request

Research-Grade Support

Dedicated service for labs, clinics, and
compounders handling RUO items.

Lab-Grade Quality Assurance

All compounds are tested for-identity and purity, COAs and supporting documentation are available upon request.

Strict RUO Compliance

All products are labeled for Researd Use Only (RUO), Not intended for human or veterinary therapeutic or diagnostic purposes.

Lab-Grade Quality Assurance

Custom branding.
white-label optionons and formulation assistancee available for eligible research institutions and partners.

Custom R&D & APl Synthesis

We support original
pharmaceutica solutions.custom research projects, and NDC-grade materials-meeting speifica.tions for qualified partners.

Serving Professionals Across the U.S.& Mexico

Trusted by MedSpas, wellness clinics and licensed compounders under licensed compounding relationships.

Secure & Discreet Fulfillment

Cold-chain shipping : private, plain.wrap packaging, and tracking for sensitive RUO materials.

⚠️ All compounds are provided strictly for Research Use Only (RUO). BLUEBIOTECH does not endorse or support clinical, therapeutic, or diagnostic use of its products unless under licensed compounder supervision.

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