FDA Label for Biofilm Blast Md
View Indications, Usage & Precautions
Biofilm Blast Md Product Label
The following document was submitted to the FDA by the labeler of this product Synergy Wound Technology, Inc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Drug Facts
Active Ingredients
Hydrogen Peroxide 1 % (v/v)
Purpose
Topical Antiseptic
Uses:
Antimicrobial skin cleanser helps reduce bacteria that potentially cause infection • For general skin and wound cleaning.
Warnings:
For external use only. Do not use in eyes. Do not ingest. Do not use if allergic to ingredients. Discontinue use if irritation, redness or pain develops. If condition persists, consult a doctor.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children; for children 2 and under consult a physician before use.
Directions For Use:
Clean wound prior to use. Shake well then apply spray evenly over skin or wound area. Repeat spray application to gauze pad then lightly "fluff" gauze and pack into open wounds as appropriate. Reapply 1 to 3 times a day, or as directed by a physician. Stop use if condition worsens.
Other Information:
Store between 20-25°C (68-77°F). Avoid direct sunlight.
Inactive Ingredients:
Purified water, silver hydrosol (proprietary)
Questions?
Packaging
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