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Eudermis Wound Care

Generic name: benzalkonium chloride
Dosage form: gel
Drug class: Antiseptic and germicides

Medically reviewed by Drugs.com. Last updated on Mar 22, 2021.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

DRUG FACTS

ACTIVE INGREDIENT ..... PURPOSE

BENZALKONIUM CHLORIDE 0.1% ..... ANTIMICROBIAL

INDICATIONS

  • FOR MANAGEMET OF STAGE 1-IV PRESSURE ULCERS, STASIS ULCERS,

DIABETIC SKIN ULCERS, POST-SURGICAL INCISIONS, FIRST AND

SECOND-DEGREE BURNS, CUTS, ABRASIONS AND SKIN IRRITATIONS.


WARNINGS

FOR EXTERNAL USE ONLY. AVOID CONTACT WITH EYES; RINSE

IMMEDIATELY WITH COOL TAP WATER IF CONTACT OCCURS.

DO NOT USE MORE THATN THE RECOMMENDED DOSE OR LONGER

THAN PRESCRIBED WITHOUT CHECKING WITH YOUR PHYSICIAN.

TALK WITH YOUR PHYSICIAN BEFORE YOU USE ANY OTHER MEDICINES

OR CLEANSERS ON YOUR SKIN. ASK YOUR PHYSICIAN BEFORE

PROLONGED SUN EXPOSURE. IF YOUR SYMPTOMS DO NOT

IMPROVE OR IF THEY WORSEN, CONTACT YOUR PHYSICIAN.

KEEP OUT OF REACH OF CHILDREN

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON

CONTROL CENTER IMMEDIATELY.

DIRECTIONS

CLEAN THE WOUND BEFORE EACH APPLICATION. APPLY A THIN

LAYER OF EUDERMIS® WOUND CARE GEL TO THE WOUND

SURFACE AND SKIN IMMEDIATELY SURROUNDING THE WOUND.

COVER THE WOUND AS DIRECTED BY YOUR PHYSICIAN.

CONTAINS EGGSHELL MEMBRANE POWDER - A NON-ALLERGENIC

ORGANIC SOURCE OF SOLUBILIZED PROTEIN TISSUE GROWTH

FACTORS INCLUDING COLLAGEN, ELASTIN, HYALURONIC ACID,

EIGHT ESSENTIAL AMINO ACIDS AND TRANSFORMING

GROWTH FACTOR - b.

Product Package

BY PRESRIPTION ONLY

BLAINE LABS®

EUDERMIS®
WOUND CARE GEL

BENZALKONIUM CHLORIDE
IN A GEL CONTAINING
TRANSFORMING GROWTH FACTOR - ß

3.0 FL OZ (88.7 mL)

MANUFACTURED BY: QUESTIONS OR COMMENTS?
BLAINE LABS, INC. CALL 800.307.8818
11037 LOCKPORT PLACE M-F, 8AM-5PM (PST)
SANTA FE SPRINGS, CA 90670

REV20190215 80000-01-TB01

res

EUDERMIS RX
benzalkonium chloride gel
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:63347-900
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.0887 g in 88.7 mL
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
EGG SHELL MEMBRANE
TROLAMINE
CARBOXYPOLYMETHYLENE
HYALURONIC ACID
ALOE VERA LEAF
PHENOXYETHANOL
METHYLPARABEN
ETHYLPARABEN
PROPYLPARABEN
BUTYLPARABEN
ISOBUTYLPARABEN
Packaging
# Item Code Package Description
1 NDC:63347-900-01 88.7 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 04/01/2019
Labeler - Blaine Labs Inc. (017314571)
Registrant - Blaine Labs Inc. (017314571)
Establishment
Name Address ID/FEI Operations
Blaine Labs Inc. 017314571 manufacture(63347-900)
Blaine Labs Inc.

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