Label: DERMAWOUND WOUND CARE VENOUS STASIS- benzocaine hydrochloride ointment
- NDC Code(s): 57554-120-06
- Packager: Progressive Doctors, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before use
- Stop use and ask a doctor if
- Keep Out of Reach of Children
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Directions
- Gently clean around 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.
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Cautions
- Persons allergic or sensitive to iodine and/or benzocaine should avoid contact with this product.
- Do not restrict circulation when applying DermaWound with sterile gauze. ®
- Apply additional sterile gauze to absorb exudates, if needed.
- Change Dressing 2 or 3 times daily or as directed by a physician.
- Other Information
- Inactive ingredients
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Questions or Comments?
www.DermaWound.com or 1-866-727-0462
Non-irritating, Clinically tested, and Allergy tested.
Certified Green Manufacturing Contents Biodegradable Eco-Friendly
Manufactured for and Distributed by Wound Care USA, LLC Tucson, Arizona 85712
©2014 U.S. & International Patents Pending
Made With Solar Power
Made in U.S.A. NDC# 57554-120-06
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INGREDIENTS AND APPEARANCE
DERMAWOUND WOUND CARE VENOUS STASIS
benzocaine hydrochloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57554-120 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 1.27 g in 100 g Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) CALCIUM CARBONATE (UNII: H0G9379FGK) GLYCERIN (UNII: PDC6A3C0OX) XANTHAN GUM (UNII: TTV12P4NEE) METHYLPARABEN (UNII: A2I8C7HI9T) WATER (UNII: 059QF0KO0R) POVIDONE-IODINE (UNII: 85H0HZU99M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57554-120-06 1 in 1 CARTON 02/02/2014 1 179 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 02/01/2014 Labeler - Progressive Doctors, LLC (623841355)