• Water based amorphous silver hydrogel
• Broad spectrum antimicrobial
• Easy to use tube
• Non-adhesive to the wound
• Rehydrates necrotic tissue and assists with autolytic debridement
• Pain free removal
• Loosens slough
• Comfortable and soothing
• Can be used to fill dead space

ZeniGEL Ag requires a prescription from a healthcare provider, for the management of dry to minimally exuding partial and full-thickness wounds, including:
• Pressure injuries
• Venous ulcers
• Diabetic ulcers
• Surgical wounds
• Donor sites
• Graft sites
• Device insertion site wounds
• Partial-thickness burns
• Traumatic wounds (such as lacerations, abrasions, and skin tears)
• Necrotic wounds (to support autolytic debridement)
• May be used on infected wounds under the supervision of a healthcare professional

ZeniGEL-Ag is contraindicated for:
• Full-thickness (third-degree) burns
• Patients with known hypersensitivity or allergy to hydrogel, silver, or any of dressing components

• Single patient use only. Do not reuse. For external use only.
• Remove prior to MRI, radiation, X-ray, ultrasound, thermotherapy and microwave diathermy.
• Do not use for longer than 14 consecutive days.
• Do not exceed 10g gel per 10kg of body weight per day.
• This dressing does not replace systemic therapy or other infection management in clinically infected wounds.
• Discontinue use if signs of irritation or sensitivity occur.

No known adverse effects or reactions.

ZeniGEL-Ag silver hydrogel should be kept in the sealed packaging. Store at room temperature in a cool, dry place. Avoid direct sunlight and excessive humidity. Dispose of used dressing per institutional policy and local regulations.

Ionic silver