Active substances
Hyaluronic acid + Lidocaine
- SFDA 8
SFDA Saudi Arabia — SFDA human drug list
| Trade name | Strength | Form · route | Pack | Public price | Type | Company | Status |
|---|---|---|---|---|---|---|---|
| TEOSYAL PureSence ULTRA DEEP | 25,0.3 mg/ml,% | Gel for injection · Subcutaneous use | 2 Pre-filled syringe | SAR 725.05 | Generic · Prescription | TeoxaneSA | Valid |
| TEOSYAL PureSense REDENSITY 2 | 15,0.3 mg/ml,% | Gel for injection · Intradermal use | 2 Pre-filled syringe | SAR 418.60 | Generic · Prescription | TeoxaneSA | Valid |
| TEOSYAL PureSense ULTIMATE | 22,0.3 mg/ml,% | Gel for injection · Subcutaneous use | 2 Pre-filled syringe | SAR 531.70 | Generic · Prescription | TeoxaneSA | Valid |
| Teosyal PureSense KISS | 25,0.3 mg/ml,% | Gel for injection · Intradermal use | 2 Pre-filled syringe | SAR 707.85 | Generic · Prescription | TeoxaneSA | Valid |
| JUVEDERM ULTRA 4 | 24, 3 mg/g | Gel · Intradermal use | 2 Pre-filled syringe | SAR 763.55 | Generic · Prescription | ALLERGAN | Withdrawn by MAH · Not Marketed |
| JUVEDERM VOLBELLA WITH LIDOCAINE | 15, 3 mg/g | Gel · Intradermal use | 2 Pre-filled syringe | SAR 1136.95 | Generic · Prescription | ALLERGAN | Withdrawn by MAH · Not Marketed |
| JUVEDERM VOLIFT WITH LIDOCAINE | 17.5, 3 mg/g | Gel · Intradermal use | 2 Pre-filled syringe | SAR 1192.90 | Generic · Prescription | ALLERGAN | Withdrawn by MAH · Not Marketed |
| JUVEDERM VOLUMA WITH LIDOCAINE | 20, 3 mg/g | Gel · Intradermal use | 2 Pre-filled syringe | SAR 1190.75 | Generic · Prescription | ALLERGAN | Withdrawn by MAH · Not Marketed |
Components
Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.