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NABOTA 150 Units (1 Vial)
4100
NABOTA 150 Units (1 Vial)
4100
Product Notice
Expiration Date — 21 May 2027
This vial is within its shelf life and fully suitable for use through the date shown above.
Product Identification
NABOTA 150 Units
Botulinum Toxin Type A — Purified Neurotoxin Complex
Daewoong Pharmaceutical Vacuum-dried Powder HI Pure Technology — Patented
Total Content / Package
150 Units × 1 Vial
Available Vial Sizes — NABOTA Series
100 Units 150 Units 200 Units
Core Ingredients & Technical Details
Primary Active Ingredient
Neuromodulator — Hall Group Strain 150 Units Clostridium botulinum toxin type A Purified neurotoxin complex · blocks acetylcholine release at the neuromuscular junction to induce localized, temporary muscle relaxation
Mechanism of Action
- Neuromuscular Blockade: Blocks the release of acetylcholine from nerve endings at the neuromuscular junction, halting muscle contractions in the targeted area.
- Localized Muscle Relaxation: Produces temporary, controlled muscle relaxation, smoothing overlying skin and reducing the appearance of dynamic wrinkles.
HI Pure Technology — Patented Purification Process A specialized purification technology designed to minimize unnecessary proteins and impurities within the toxin complex, thereby significantly reducing the risk of immunogenicity (toxin resistance) and improving long-term treatment reliability.
Botulinum Toxin Type A Hall Group Strain HI Pure Technology Minimized Immunogenicity Vacuum-dried Powder
Efficacy & Expected Benefits
Main Effects
- Deep wrinkle correction — effectively diminishes dynamic wrinkles by restricting excessive muscle movement
- Temporary muscle relaxation for facial and body contouring
- Relief of muscle spasticity in therapeutic applications
Recommended Treatment Areas
Glabellar Lines (Frown Lines) Crow's Feet Forehead Wrinkles Masseter — Jawline Slimming Calves Arms Upper Limb Spasticity
Dosage Guide by Treatment Area
| Treatment Area | Total Units | Volume / Site | Injection Sites | Notes |
|---|---|---|---|---|
| Glabellar Lines | 20 U | 0.1 mL (4 U) per site | 5 sites (corrugator & procerus) | Standard frown line protocol |
| Crow's Feet | 24 U | Divided per side | 3 sites per side (12 U per side) | Bilateral treatment |
| Masseter (Jawline) | 50–100 U | Variable | Variable | Bilateral; adjust to muscle size |
| Muscle Spasticity | Up to 360 U total | Variable | Divided across affected muscles | Dose by muscle size & severity |
Dosage references are provided as general clinical guidelines. Actual dosing must be determined by the treating physician based on individual patient assessment.
Usage Protocol & Application Guide
Application Method
Intramuscular injection using a fine needle — 30–33 gauge recommended for superficial facial muscles.
Treatment Cycle
Sessions spaced every 3–6 months. Frequent or premature re-administration is not recommended to avoid the development of toxin resistance.
Onset & Duration of Effect
| Timepoint | Observable Effect |
|---|---|
| Day 1–2 | Initial chemical denervation begins |
| First Week | Effects peak in intensity |
| 3–6 Months | Full therapeutic and aesthetic effects — duration varies by treated area |
Reconstitution Instructions
-
1 Reconstitute using 0.9% preservative-free sterile sodium chloride (saline) solution.
-
2 Insert the needle and direct the diluent slowly against the vial wall to prevent foaming.
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3 Gently swirl the vial to mix. Do not shake vigorously — agitation can degrade the active toxin proteins.
Storage & Handling
Required Storage Temperature
Refrigerated: 2–8°C · Keep sealed until use
After Reconstitution
Store in refrigerator (2–8°C) and use within 24 hours.
General Handling Tips
- Ship in insulated packaging with ice packs to maintain cold chain integrity.
- Do not shake the vial vigorously at any stage — agitation degrades active toxin proteins.
Precautions & Safety Notes
Contraindications Contraindicated during pregnancy or breastfeeding, in patients with known hypersensitivity to botulinum toxin type A, and in patients with neuromuscular junction disorders (e.g., Myasthenia Gravis, ALS).
Safety Warnings Professional medical use only. Precise dosing and anatomical placement are critical — improper injection may cause ptosis (drooping eyelids), uneven eyebrow position, or toxin extravasation to adjacent muscles. Do not inject into blood vessels.
Common Temporary Side Effects
Note Swelling, bruising, pain or tenderness at the injection site, redness, and temporary localized muscle weakness may occur following treatment.
Post-Treatment Care
-
1 Remain upright for at least 4 hours following injection.
-
2 Avoid touching, rubbing, or massaging the treated areas for at least 4 hours to prevent toxin migration to adjacent muscles.
-
3 Refrain from strenuous exercise, saunas, and excessive heat exposure for 24 hours post-injection.
Keywords & Search Terms
NABOTA 150U Botulinum Toxin Type A Daewoong Pharmaceutical HI Pure Technology Neuromodulator Wrinkle Reduction Glabellar Lines Masseter Reduction Muscle Spasticity Crow's Feet Injectable Korean Botox Jawline Slimming
Lipotocin Inj (12mL x 10 Amps)
4100
Lipotocin Inj (12mL x 10 Amps)
4100
Product Identification
Lipotocin Inj.
High Dose Cinderella Injection
South Korean Manufacturer IV Injection Ampoule
Total Volume/Content
120mL per box (12mL × 10 Ampoules)
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technology
Primary Active Ingredients
Thioctic Acid (Alpha-Lipoic Acid) 300mg
Mechanism of Action
Thioctic Acid acts as an antioxidant master, regenerating Vitamin C, E, and Glutathione while scavenging free radicals. It also increases mitochondrial energy expenditure to aid in lipolysis (fat breakdown) and prevents protein glycation to reduce tissue aging.
Thioctic Acid 300mg High Dose Metabolic Activation Anti-Glycation
Efficacy & Benefits
Main Effects
- Intensive Anti-Aging: Powerful antioxidant protection against cellular damage.
- Skin Brightening: Reduces dullness and improves skin texture ("Baby Face Injection").
- Body Slimming: Boosts metabolism to aid in weight loss and reduce edema.
- Fatigue Recovery: Improves energy levels and exhaustion.
- Diabetic Neuropathy Relief: Relieves sensory abnormalities.
Targeted Use
Systemic IV Drip Skin Tone Improvement Metabolic Boost
Usage Protocol
Dilution Required Do not inject undiluted directly ("IV Push") as it causes vascular pain and potential shock.
Application Method
Intravenous Drip (IV Infusion)
Dilution Protocol
Mix 1 ampoule (12mL) with 100mL – 250mL of Normal Saline.
Infusion Speed
Administer slowly over at least 15–30 minutes.
Treatment Cycle
1–2 times per week; standard course of 10 sessions.
Product Comparison
| Product Version | Thioctic Acid Content | Primary Strategy |
|---|---|---|
| Lipotocin (High Dose) | 300mg / 12mL | Intensive Slimming & Metabolic Boost |
| Standard Cindella (Low Dose) | 25mg / 5mL | Cocktail Maintenance (Mixed with Vit C/Glutathione) |
Storage & Handling
Required Storage Temperature
Room temperature (1°C – 30°C)
Light Sensitivity
Strictly Protect from Light. Keep ampoules in the original box until use.
Shelf Life
24–36 months from manufacture date
Precautions & Safety
Contraindications Do not use in children/adolescents or patients with hypersensitivity to Thioctic Acid.
Safety Warnings Rapid infusion can cause headache, nausea, and respiratory distress. Diabetics should monitor glucose levels as Thioctic acid may cause hypoglycemia.
Common Temporary Side Effects
- Nausea, vomiting, or gastrointestinal discomfort (rare with slow drip).
- Skin rash or itching at the injection site.
Post-Treatment Care
Avoid heavy alcohol consumption as it interferes with metabolic effects.
Frequently Asked Questions
What is Lipotocin Inj. used for?
Lipotocin Inj. is a high-dose Thioctic Acid (Cinderella) injection used for intensive anti-aging antioxidant protection, skin brightening, body slimming through metabolic boost and edema reduction, fatigue recovery, and relief of diabetic neuropathy (sensory abnormalities).
What is Lipotocin's active ingredient?
The primary active ingredient is Thioctic Acid (Alpha-Lipoic Acid) at 300mg per 12mL ampoule. It acts as an antioxidant master, regenerating Vitamins C and E and Glutathione, increasing mitochondrial energy expenditure to aid lipolysis, and preventing protein glycation.
How is Lipotocin administered?
Lipotocin is administered as an intravenous drip (IV infusion). One ampoule (12mL) is diluted with 100mL–250mL of normal saline and infused slowly over at least 15–30 minutes. It must not be injected undiluted as an IV push, which can cause vascular pain and potential shock. The standard cycle is 1–2 times per week for a course of 10 sessions.
Who should not use Lipotocin and what are the precautions?
Lipotocin is contraindicated in children and adolescents and in patients with hypersensitivity to Thioctic Acid. Rapid infusion can cause headache, nausea, and respiratory distress, and diabetics should monitor glucose levels as Thioctic Acid may cause hypoglycemia. Heavy alcohol consumption should be avoided as it interferes with the metabolic effects.
Keywords
Lipotocin Thioctic Acid 300mg Alpha Lipoic Acid High Dose Cindella Cinderella Injection Fat Burn Injection Antioxidant IV Metabolism Booster