PURITOX® 100 UNITS
PURITOX® 100 Units – Professional Botulinum Toxin Type A
Precision. Purity. Performance.
PURITOX® 100 Units is a professional Botulinum Toxin Type A product developed for physicians, dermatology professionals, plastic surgeons, and qualified medical-aesthetic providers seeking precision, consistency, and controlled clinical performance.
Manufactured using advanced purification technology, PURITOX® is designed to provide a highly refined toxin profile with reduced unnecessary complexing proteins. This supports controlled diffusion, precise neuromuscular targeting, and predictable professional results.
The 100 Unit vial offers a practical format for facial aesthetic procedures, individualized patient treatments, and clinics seeking efficient inventory management without the larger volume of a 100 Unit vial.
Why Professionals Choose PURITOX®
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High-Purity Formulation
A highly refined Botulinum Toxin Type A formulation designed to support precise application and consistent professional performance.
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Controlled Diffusion
Designed to support targeted treatment placement while helping providers maintain control over the intended treatment area.
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Predictable Aesthetic Outcomes
Supports the temporary softening of dynamic facial lines while helping maintain natural-looking facial movement and expression.
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Professional Practice Efficiency
The 100 Unit vial is well suited for individual aesthetic appointments, lower-volume treatment days, and practices that prefer a smaller vial format.
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Flexible Professional Application
May be used across physician-directed aesthetic or therapeutic protocols according to professional judgment, training, labeling, and applicable regulations.
Common Professional Applications
Aesthetic Applications
- Temporary improvement in the appearance of dynamic facial lines
- Glabellar line treatment
- Forehead line treatment
- Lateral canthal line treatment
- Physician-directed facial contouring procedures
- Masseter and jawline-related aesthetic protocols
- Other qualified provider-directed cosmetic applications
Therapeutic Applications
- Physician-directed hyperhidrosis protocols
- Selected neuromuscular applications
- Muscle hypertrophy management under medical supervision
- Other qualified provider-directed therapeutic applications
Designed for Practice Efficiency
- 100 Unit vial format
- Vacuum-dried lyophilized powder
- Suitable for individualized professional treatment planning
- Efficient option for facial aesthetic procedures
- Supports flexible professional reconstitution protocols
- Designed for refrigerated professional storage
Packaging
Supplied as a sterile, single-use vial containing 100 Units of vacuum-dried, lyophilized Botulinum Toxin Type A.
For Licensed Medical Professionals Only
PURITOX® must be purchased, prepared, and administered only by an appropriately licensed and trained healthcare professional.
PURITOX® must be purchased, prepared, and administered only by an appropriately licensed and trained healthcare professional.
Existing Dermafirm USA professional account holders should log in to view professional purchasing options.
New professional customers may submit an application through the Dermafirm USA professional registration page.
Register for a Professional AccountProfessional Preparation and Administration
PURITOX® 100 Units is intended only for administration by licensed healthcare professionals trained in Botulinum Toxin Type A preparation, facial anatomy, injection techniques, emergency procedures, and complication management.
Before Use
- Confirm the product name, vial strength, lot number, expiration date, and package integrity.
- Verify that the vial has been transported and stored under the required refrigerated conditions.
- Review the client’s medical history, allergies, medications, previous Botulinum Toxin treatments, treatment goals, and contraindications.
- Obtain appropriate informed consent before treatment.
- Confirm that treatment is permitted within the provider’s professional license and applicable jurisdiction.
General Reconstitution Procedure
- Remove the PURITOX® 100 Unit vial from refrigerated storage according to the official product instructions.
- Inspect the vial carefully. Do not use a vial that is damaged, compromised, expired, or improperly stored.
- Clean the vial stopper using an appropriate antiseptic technique and allow it to dry.
- Use only the manufacturer-specified sterile diluent and follow the official prescribing information for the selected concentration.
- Introduce the diluent slowly and carefully into the vial using aseptic technique.
- Gently rotate or swirl the vial as directed. Do not shake the vial.
- Inspect the reconstituted solution before use. Do not administer if the solution contains unexpected discoloration, visible particles, or precipitate.
- Label the reconstituted vial with the date, time, concentration, and preparer information according to facility policy.
Professional Administration
- Determine the treatment plan based on the client’s anatomy, muscle activity, treatment history, and clinical goals.
- Select the appropriate concentration, dose, injection depth, and treatment sites according to the official product labeling and the provider’s professional judgment.
- Use appropriate aseptic technique throughout preparation and administration.
- Avoid exceeding product-specific or patient-specific dosing limitations.
- Monitor the client during and after treatment for immediate adverse reactions.
- Document the total units administered, concentration, injection sites, lot number, expiration date, and client response.
After Treatment
- Provide the client with written post-treatment instructions.
- Explain expected treatment response, follow-up timing, and signs that require medical evaluation.
- Schedule follow-up according to the provider’s established clinical protocol.
- Store or discard any remaining product strictly according to the official manufacturer instructions and facility requirements.
Storage
- Store unopened vials under the refrigerated conditions stated on the official product label.
- Protect the product from inappropriate temperatures and unauthorized access.
- Follow the official instructions regarding the allowable storage period after reconstitution.
- Do not use product that has been frozen, overheated, contaminated, or stored outside the required conditions.
Important:
The exact reconstitution volume, concentration, dosage, injection placement, treatment interval, and post-reconstitution storage period must be determined from the official PURITOX® 100 product labeling and by the treating licensed healthcare professional. Units of Botulinum Toxin products may not be interchangeable across different manufacturers.
The exact reconstitution volume, concentration, dosage, injection placement, treatment interval, and post-reconstitution storage period must be determined from the official PURITOX® 100 product labeling and by the treating licensed healthcare professional. Units of Botulinum Toxin products may not be interchangeable across different manufacturers.
Ingredients and Product Information
| Product Name | PURITOX® 100 Units |
| Active Ingredient | Botulinum Toxin Type A |
| Vial Strength | 100 Units per vial |
| Dosage Form | Vacuum-dried, lyophilized powder for professional reconstitution |
| Administration | For administration by appropriately licensed and trained healthcare professionals |
| Packaging | Sterile, single-use vial |
| Appearance Before Reconstitution | Lyophilized powder contained within the vial |
| Appearance After Reconstitution | The prepared solution should meet the appearance requirements stated in the official manufacturer instructions |
| Storage | Refrigerate according to the temperature range printed on the official product packaging |
| Intended User | Licensed healthcare professionals only |
Inactive Ingredients
Refer to the official PURITOX® 100 package insert or manufacturer-issued product documentation for the complete and authoritative list of excipients and inactive ingredients.
Do not assume that the inactive ingredients in PURITOX® 100 are identical to those of another Botulinum Toxin Type A product.
Important Product Information
- For professional medical use only.
- The product must be prepared and administered using appropriate aseptic technique.
- Botulinum Toxin potency units are specific to the manufacturer’s assay and should not be converted directly to units of another product.
- Review the official product labeling for contraindications, warnings, adverse reactions, dosing limitations, and storage requirements.
- Do not use if the vial, seal, labeling, or product integrity appears compromised.
Professional Medical Disclaimer: The information on this page is provided for general professional product education and does not replace the official product insert, prescribing information, manufacturer instructions, clinical training, or independent medical judgment. PURITOX® 100 Units must be purchased, prescribed, prepared, and administered only as permitted by applicable laws and by an appropriately licensed healthcare professional.