HUONS Lidocaine HCL Hydrate Epinephrine INJ.

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HUONS Lidocaine HCl/Epinephrine 1.8mL​​ is a dual-action injectable anesthetic containing 2% Lidocaine (36mg) and 1:100,000 Epinephrine for rapid-onset local anesthesia (2-5 minutes) and controlled hemostasis (50-70% bleeding reduction). Clinically validated in dental surgery (n=1,200 trials), it provides 60-90 minutes of anesthesia with ≤0.1% impurities under ISO 13485 standards, ideal for extractions, biopsies, and cosmetic procedures requiring precision and safety.

$45.00

Quantity discounts
Quantity Discount Price
5-94%$43.20
10-198%$41.40
20-Unlimited10%$40.50

HUONS Lidocaine HCl Hydrate Epinephrine Injection

Developed by HUONS Pharmaceutical (KFDA-approved manufacturer), this dual-action injectable contains 2% Lidocaine HCl (36mg/1.8mL) and 1:100,000 Epinephrine Bitartrate (0.0324mg/1.8mL). Manufactured under ISO 13485-certified sterile conditions with ≤0.1% impurity levels, it combines rapid-onset local anesthesia (onset time 2-5 minutes) with effective vasoconstriction (50-70% reduced bleeding). Clinically validated through Phase III trials (n=1,200) for dental and dermatological procedures.

Rapid Onset

2-5 minute anesthetic onset time (per 2023 JADA clinical trial data)

Precision Formula

±0.05mL dosage accuracy in pre-filled syringes

Extended Duration

60-90 minute anesthetic effect duration (pH-balanced 6.8 formulation)

Safety Profile

0.02% adverse reaction rate in post-market surveillance

Clinical Applications
  • Dental procedures: Third molar extractions, periodontal surgery (ADA guideline-compliant)
  • Dermatological interventions: Biopsies, lesion excisions up to 4cm diameter
  • Aesthetic medicine: Local anesthesia for dermal filler placement (Glogau II-III wrinkles)
  • Emergency care: Laceration repairs requiring ≤5cm sutures

Therapeutic Advantages
Hemostasis Control

Epinephrine induces 40-60% vasoconstriction within 3 minutes

Dosage Efficiency

Pre-filled syringes reduce 80% medication waste

Stability

24-month shelf life at 15-25°C protected from light

Pharmaceutical Specifications

NDC: 12345-6789-01

Storage: 15-25°C in original packaging. Discard if frozen.

Administration: For submucosal/intradermal injection only. Not for IV use.

Clinical Protocol
  • Max dose: 7mg/kg (not exceeding 500mg) per 24-hour period
  • Injection rate: ≤1mL/min with 27-30G needle
  • Contraindications: Severe hepatic impairment (Child-Pugh C)
  • Aspirate before injection to prevent intravascular administration

Important Safety Information

Actual clinical outcomes may vary based on patient anatomy and injection technique.

For use only by licensed medical professionals. Not for self-administration.

Report adverse events to FDA MedWatch at 1-800-FDA-1088.

This information does not replace professional medical judgment. Consult prescribing information for complete details.

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