BioFilm Blast MD

Manufacturer
Synergy Wound Technology, Inc
Effective date
2025-07-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:35:22

Label at a glance#

ProductBioFilm Blast MD
Active ingredientHYDROGEN PEROXIDE
Label structure10 sections

Indications and uses

Antimicrobial skin cleanser helps reduce bacteria that potentially cause infection • For general skin and wound cleaning.

Dosage and administration

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.

Storage and handling

Store between 20-25°C (68-77°F). Avoid direct sunlight.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Hydrogen Peroxide 1 % (v/v)

Purpose

OTC - PURPOSE SECTION

Topical Antiseptic

Uses:

INDICATIONS & USAGE SECTION

Antimicrobial skin cleanser helps reduce bacteria that potentially cause infection • For general skin and wound cleaning.

Warnings:

WARNINGS SECTION

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 SECTION

Keep out of reach of children;for children 2 and under consult a physician before use.

Directions for Use:

DOSAGE & ADMINISTRATION SECTION

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:

STORAGE AND HANDLING SECTION

Store between 20-25°C (68-77°F). Avoid direct sunlight.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Purified water, silver hydrosol (proprietary)

Questions?

OTC - QUESTIONS SECTION

info@biofilmblastmd.com

SPL UNCLASSIFIED SECTION

www.biofilmblastmd.com

• Skin and Wound Cleanser

• Helps Prevent Infection

Distributed by InteliWound. San Diego, CA 92131

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Synergy-401Synergy-401

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83279-401-102025-07-30C16284748780-13b156c62-2e99-fb37-e063-e6dba90a4e07BioFilm Blast MD TM

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83279-40183279-401-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SILVER3M4G523W1GIACT
HYDROGEN PEROXIDEBBX060AN9VACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3b28a1d7-06e8-fdb8-e063-6294a90acae4404916b6-7e97-42fd-ab73-7b6d75c1d8ff2025-07-30WarningsExact identifier
spl id: 3b28a1d7-06e8-fdb8-e063-6294a90acae4
spl set id: 404916b6-7e97-42fd-ab73-7b6d75c1d8ff

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.