ANTISEPTIC BANDAGES- benzalkonium chloride dressing 
Pharmaplast SAE

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Cure Aid Topical antimicrobial adhesive bandages

Drug Facts

Active ingredients

Benzalkonium Chloride 0.1%

Purpose

Topical antimicrobial adhesive bandage

Uses

First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

Warnings

  • For external use only.
  • Stop use and consult a doctor if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.

  • Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions

Clean and dry the affected area. Apply a sterile bandage on the area 1 to 3 times daily.

Inactive Ingredients

None

CURE-AID®

INTENDED USE:
Antimicrobial Adhesive Bandages are to be applied to the skin for topical application. The bandages help provide an antibacterial barrier for minor cuts and scrapes.

DIRECTIONS:
Apply bandages to clean, dry skin. Change daily or when pad becomes wet. Sterile unless wrapper is damaged or open.

WARNINGS:
FOR MEDICAL EMERGENCIES SEEK PROFESSIONAL HELP

GERM FIGHTING PROTECTION
• Help prevent infection • Safe for all minor cuts and scrapes • Unique, long lasting adhesive • Medicated non-stick pad

  • Each strip has been sealed and sterilized for your protection.
  • Be sure skin is clean and dry before applying. Change bandage as needed.
  • Sterility guaranteed unless individual envelope has been opened or damaged.

Pharmaplast

Amria – Alexandria
Egypt
www.Pharmaplast-online.com

Packaging

labellabel

ANTISEPTIC BANDAGES 
benzalkonium chloride dressing
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:28691-0010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Other Ingredients
Ingredient KindIngredient NameQuantity
Does not containNATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN) 0 mg  in 100 mg
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:28691-0010-520 in 1 BOX10/07/201605/23/2024
10.033 mg in 1 PATCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
2NDC:28691-0010-630 in 1 BOX10/07/201605/23/2024
20.033 mg in 1 PATCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
3NDC:28691-0010-740 in 1 BOX10/07/201605/23/2024
30.033 mg in 1 PATCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)10/07/201605/23/2024
Labeler - Pharmaplast SAE (644773319)
Establishment
NameAddressID/FEIBusiness Operations
Pharmaplast SAE644773319analysis(28691-0010) , label(28691-0010) , manufacture(28691-0010) , pack(28691-0010)

Revised: 5/2024
Document Id: c32ebe1b-c8eb-4c3b-9512-881fd83351f5
Set id: ce7af871-a38d-4c51-8b0e-cb0eec5e8554
Version: 5
Effective Time: 20240524
 
Pharmaplast SAE