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Bionect Cream, Gel (Hyaluronic acid sodium salt): Side Effects, Uses, Dosage, Interactions, Warnings

Bionect

Last updated on RxList: 1/28/2021

Drug Summary

What Is Bionect?

Bionect (hyaluronic acid sodium salt) cream and gel is a biological polysaccharide indicated for the dressing and management of partial to full thickness dermal ulcers (pressure sores, venous stasis ulcers, arterial ulcers, diabetic ulcers), wounds including cuts, abrasions, donor sites, and is intended to cover a wound or burn on a patient's skin, and protect against abrasion, friction, and dryness.

What Are Side Effects of Bionect?

Side effects of Bionect include sensitization to the drug. A side effect of Bionect oral gel is a burning sensation in your mouth. Serious side effects of Bionect include allergic reactions such as skin irritation, rash, hives, itching, swelling (especially of the face, tongue or throat), severe dizziness, trouble breathing, or tightness of the chest.

Dosage for Bionect

Bionect is available as a cream or gel in strength of 0.2% hyaluronic acid sodium salt. Bionect should be applied in a thin layer without extensive rubbing onto the wound surface, two or three times per day. Cover the lesion area with a sterile gauze pad and, if necessary, with an elastic or compressive bandage. If condition worsens, consult your physician immediately. Keep this product out of the reach of children. Each tube of Bionect should be used by one patient only in order to reduce the risk of cross infection. Do not use the product after the expiration date reported on the package.

What Drugs, Substances, or Supplements Interact with Bionect?

Bionect may interact with other drugs. Tell your doctor all medications and supplements you use.

Bionect During Pregnancy and Breastfeeding

No information is available with regard to pregnancy or nursing while using Bionect. Use of this drug in pediatric patients has been done experimentally.

Additional Information

Our Bionect Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.

For topical use only

Description for Bionect Cream, Gel

BIONECT® Cream is a white, viscous cream. BIONECT® Gel is a clear, colorless gel. The principal component is the sodium salt of hyaluronic acid (0.2%). Hyaluronic acid is a biological polysaccharide (glycosaminoglycan) and is a major component of the extracellular matrix of connective tissues.

Ingredients

BIONECT® Cream - Hyaluronic acid sodium salt (Hyalastine®), polyethyleneglycol 400 monostearate, decyl ester of oleic acid, emulsifying wax, glycerol, sorbitol solution 70%, sodium dehydroacetate, methylparaben, propylparaben, fragrance, purified water. BIONECT® Cel - Hyaluronic acid sodium salt, sorbitol solution 70%, sodium dehydroacetate, methylparaben, propylparaben, carbomer 980, sodium hydroxide, purified water.

Uses for Bionect Cream, Gel

BIONECT® is indicated for the dressing and management of partial to full thickness dermal ulcers (pressure sores, venous stasis ulcers, arterial ulcers, diabetic ulcers), wounds including cuts, abrasions, donor sites, and post-operative incisions, irritations of the skin, and first and second degree burns. The dressing is intended to cover a wound or burn on a patient's skin, and protect against abrasion, friction, and desiccation.

Dosage for Bionect Cream, Gel

The wounds or ulcers should be cleaned and disinfected prior to treatment. In the event of long-standing ulcers, it may be advisable to clean and/or to debride the wound by surgical or enzymatic means, prior to treatment. Apply a thin layer of BIONECT® without extensive rubbing onto the wound surface, two or three times per day. Cover the lesion area with a sterile gauze pad and, if necessary, with an elastic or compressive bandage.

HOW SUPPLIED

BIONECT® Cream/Gel is supplied in a:

25g tube (Cream) - NDC 68712-007-02
30g tube (Gel) - NDC 68712-008-02
60g (2 - 30g Gel tubes) - NDC 68712-008-03

Storage

Please store BIONECT® at room temperature.
BIONECT® Cream may be stored for up to 24 months, BIONECT® Gel may be stored for up to 24 months.

Manufactured for: JSJ Pharmaceuticals, Inc. 140 East Bay Street, Charleston, SC 29401. Toll Free: 1-800-499-4468. Manufactured by: Fidia Farmaceutici S.p.A. Italy. July 2008

Side Effects for Bionect Cream, Gel

All suspected adverse reactions occurring during the treatment with BIONECT® should be reported to your doctor.

Drug Interactions for Bionect Cream, Gel

Do not use concomitantly with disinfectants containing quaternary ammonium salts because hyaluronic acid can precipitate in their presence. The concomitant topical treatment of wounds with antibiotics or other local agents has never given rise to interactions or incompatibilities with BIONECT®.

Warnings for Bionect Cream, Gel

If condition worsens, consult your physician immediately. Keep this product out of the reach of children. The prolonged use of the product may give rise to sensitization phenomena. Should this happen, discontinue the treatment and follow a suitable therapy. Do not use the product after the expiration date reported on the package.

Precautions for Bionect Cream, Gel

Each tube of BIONECT® should be used by one patient only in order to reduce the risk of cross infection.

Overdose Information for Bionect Cream, Gel

No information provided.

Contraindications for Bionect Cream, Gel

Do not administer to patients with known hypersensitivity to this product.

Clinical Pharmacology for Bionect Cream, Gel

No information provided.

Patient Information for Bionect Cream, Gel

No information provided. Please refer to the WARNINGS and PRECAUTIONS sections.

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Report Problems to the Food and Drug Administration

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.