Label: BIONECT FOAM-

  • Category: PRESCRIPTION MEDICAL DEVICE LABEL
  • DEA Schedule: None
  • Marketing Status: Premarket Notification

Drug Label Information

Updated September 8, 2014

If you are a consumer or patient please visit this version.

  • Description:

    Bionect Foam is a soft white foam, which, at rest, takes the form of a clear, pale yellow liquid.  The principal component is the sodium salt of hyaluronic acid (0.2%).  The sodium hyaluronate (Hyalastine) is derived from a natural fermentation process.  Hyaluronic acid is a biological polysaccharide (glycosaminoglycan) and is a major component of the extracellular matric of the connective tissues. 

  • Indications:

    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.

  • Directions:

    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.

  • Warnings:

    If conditions 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 expiration date reported on the package.

  • Ingredients:

    Hyaluronic acid sodium salt, purified water, butane, propylene glycol, polysorbate 80, polyvinylpyrrolidone, propane, methylparaben, sodium dehydroacetate, propylparaben. 

  • Contraindications:

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

  • Interactions:

    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.

  • Precautions:

    Avoid direct contact of container with the affected area. Each container of Bionect should be used by one patient only in order to reduce the risk of cross infection.

    Warning

    Bionect Foam - contents under preassure, do not puncture or incinerate. Do not store at temperatures above 120F. Protect from freezing. Keep out of reach of children

  • Adverse Reactions:

    All suspected adverse reactions occurring during the treatment with Bionect should be report to your doctor.

  • How Supplied:

    Bionect Foam is supplied in a 113.4g can - 68712-046-01

  • Storage:

    Please store Bionect at room temperature. Bionect Foam may be stored for up to 24 months under these conditions. Store at room temperature below 86F (30C).

    Manufactured for: Fidia Farmaceutici S.p.A - Italy

    Distributed by: Innocutis Holdings, LLC

    Charleston SC 29401

    800-499-4468

    www.innocutis.com

    www.bionect.com

    U.S. Pat. No.: 5,925,626

  • Packaging:

    Label

  • INGREDIENTS AND APPEARANCE
    BIONECT FOAM 
    dressing, wound and burn, hydrogel w/drug and/or biologic
    Product Information
    Product TypePRESCRIPTION MEDICAL DEVICEItem Code (Source)NHRIC:68712-046
    Inactive Ingredients
    Ingredient NameStrength
    HYALURONIC ACID (UNII: S270N0TRQY) 0.2 
    WATER (UNII: 059QF0KO0R)  
    BUTANE (UNII: 6LV4FOR43R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    POVIDONE (UNII: FZ989GH94E)  
    PROPANE (UNII: T75W9911L6)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NHRIC:68712-046-011 in 1 CAN
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    premarket notificationK97372209/08/2014
    Labeler - Innocutis Holdings LLC (451549861)