Hygel™
(Sodium Hyaluronate) 2.5% Rx Only
The following Structured Product Label (SPL) was submitted to the FDA by Gentex Pharma, Llc for the product Hygel (NDC 15014-105). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding hygel™, product description, ingredient, other ingredients, indications for userx only:under the supervision of a healthcare professional;, contraindications, warnings, precautions and observationsrx only:consult a healthcare professional if;, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
(Sodium Hyaluronate) 2.5% Rx Only
HyGel™ is a clear viscous, odorless, aqueous gel composed principally of sodium hyaluronate, a derivative salt of Hyaluronic acid. The portion of sodium hyaluronate “w/w” in the formulation is 2.5%.
Hyaluronic acid is a molecule which is normally found in various parts of the body. Hyaluronic acid used in HyGel™ is derived from a synthetic source more specifically from a bacterial fermentation process. HyGel™ serves to maintain a moist wound environment. The maintenance of a moist wound environment is widely recognized to positively contribute to wound healing process.
Sodium hyaluronate (2.5%)
Other ingredients in HyGel™ are as follows:
Hydroxyethyl cellulose, methylparaben, as well as polyethylene glycol, and purified water, USP.
Do not administer to patients with known hyper-sensitivity to the components of this product.
1. Signs of infection occur, increased pain, bleeding or wound drainage.
2. There is a change in wound color and/or odor.
3. The wound does not begin to show signs of healing in a few days.
4. Any other unexpected symptoms occur.
• The treatment of any leg ulcers, pressure ulcers, diabetic ulcers and surgically debrided wounds should be under the supervision of a healthcare professional.
• Appropriate supportive measures should be taken where indicated (e.g. use of graduated compression bandaging in the management of venous leg ulcers or pressure relief measures in the management of pressure ulcers).
NOTE: The control of blood glucose as well as appropriate pressure relief measures should be provided with diabetic foot ulcers.
• If the wound becomes infected, please immediately consult with a healthcare professional as to whether use of HyGel™ should be continued.
• HyGel™ is for external use only.
For Wounds;
1. First, clean the ulcer or other wound with normal saline solution (other cleaning agents are not recommended). Normal saline solution can be obtained through your location pharmacy.
NOTE: Debridement (surgical cleaning) of the wound may be performed at the discretion of the healthcare professional.
2. Remove excess moisture with a dry gauze.
3. Apply HyGel™ liberally into the cavity of the ulcer or wound site and the surrounding area.
4. Apply a non-stick gauze dressing over the wound site.
NOTE: Once HyGel™ is applied the gel should not be touched.
5. Finally, wrap a self-adhesive bandage over the non-stick gauze dressing.
6. Repeat the entire process of wound cleaning, applying HyGel™, and bandaging daily, or as needed.
7. Visit a healthcare professional as recommended.
For Dermatoses;
1. Using a few gentle strokes to smooth the gel across the skin in the same direction as hair growth, apply to the affected areas of the skin on a regular basis and as often as required.
2. If necessary, allow time for any excess to penetrate into the skin. Do not rub the skin vigorously.
3. You can apply HyGel before and after washing; showering or having a bath to help condition your skin and stop it from drying further.
4. If you are applying another topical treatment to the same areas of skin, try to avoid mixing the two products. You may choose to apply the treatments alternately, leaving sufficient time to allow the previous application to penetrate the skin.
HyGel™ is available in a 10 gram single tube with tamper evident seal, NDC 15014-105-10, a carton with four 10 gram tubes with tamper evident seal, NDC 15014-105-40, and a 75 gram tube with tamper evident seal, NDC 15014-105-75. Do not use if tamper evident foil seal is broken or missing.
Lot number and expiry date are located on the crimped end of the tube.
Store in a cool dry place; at room temperature. Temperature should not exceed 35°C/95°F. Protect from freezing.
* Please review the disclaimer below.