DermaWound Wound Care

DermaWound Wound Care is an FDA drug label for the active ingredient POVIDONE-IODINE manufactured by Progressive Doctors, LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231215.

Generic: POVIDONE-IODINE

Manufacturer: Progressive Doctors, LLC

Product Type: HUMAN OTC DRUG

Route: TOPICAL

Dosage Form:

NDC: 57554-110

Application: M003

Effective: 20231215

Active Ingredients: Active ingredient Povidone-iodine 10% (0.65% available iodine)

Indications & Usage

Uses first aid antiseptic to help prevent infection in minor cuts scrapes burns

Dosage & Administration

Directions Gently clean the affected area Prior to application of DermaWound , evaluate the wound or ulcer to insure no excessive bleeding is present. Never wipe out the ulcer. ® Apply a moderate amount of DermaWound directly to affected area. ® Deeper or "tunneling" wounds may require packing and/or sides coated with additional DermaWound and sterile gauze. ® Apply additional sterile gauze to absorb exudates, if needed. Change Dressing 2 or 3 times daily or as directed by a physician. May require supervision of a health care professional in the management of chronic & acute wound care, pressure sores, diabetic ulcers, surgical wounds & indwelling catheters.

Contraindications

Not available.

Warnings

Warnings For external use only

Adverse Reactions

Not available.

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