• Water based amorphous hydrogel in syringe applicator
• Easy to use syringe
• 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 is indicated for the management of dry or minimally exuding partial and full thickness wounds, including:
• Pressure injuries
• Venous leg ulcers
• Diabetic foot ulcers
• Surgical wounds
• Donor sites
• 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 is contraindicated for:
• Full-thickness (third-degree) burns
• Patients with known hypersensitivity or allergy to any dressing components

• Single patient use only. Do not reuse.
• Avoid application to intact peri-wound skin to reduce the risk of maceration.
• Remove prior to MRI, radiation therapy, X-ray, ultrasound, thermotherapy or microwave diathermy.
• Do not use for longer than 30 days consecutive days.
• If wound exudate increases to moderate or heavy levels, use an absorbent dressing instead of hydrogel.
• Discontinue use if signs of irritation or sensitivity occur.

No known adverse effects or reactions.

ZeniGEL amorphous 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.