Excellagen is a highly refined fibrillar bovine Type I collagen-based topical gel designed for physician use during debridement procedures, and is engineered to support a favorable wound healing environment for non-healing lower extremity ulcers in diabetic patients.
Excellagen is stored at standard refrigeration temperatures (2°C - 8°C) and is packaged in single-use 1.0cc syringes containing 0.5cc of formulated collagen, supplied with single-use sterile flexible applicator tips.
Excellagen is labeled for use by health care professionals in a clinical setting.
Excellagen is indicated for the management of wounds including partial and full thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/ undermined wounds, surgical wounds (donor sites/grafts, post-Moh's surgery, post-laser surgery, podiatric, wound dehiscence), trauma wounds (abrasions, lacerations, second-degree burns, and skin tears) and draining wounds. Excellagen is contraindicated for individuals with a known sensitivity to products of bovine origin.
Excellagen is for use by healthcare professionals in the United States. All information, including the prescribing information for Excellagen, follows laws, regulatory requirements, and medical practices for the United States only and may not be appropriate for use outside of the United States.