Medication Guide App

Bedside-Care Perineal Wash

Dosage form: liquid
Ingredients: BENZETHONIUM CHLORIDE 1mL in 1L
Labeler: Coloplast Manufacturing US, LLC
NDC Code: 11701-059

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Bedside-Care® Perineal Wash
Perineal Skin Cleanser
No-Rinse
Incontinent Cleanser

For Perineal Clean-Up

Drug Facts

Active ingredient

Benzethonium Chloride 0.1%

Purpose

Antiseptic

Uses Protects against the risk of bacterial contamination in minor cuts, scrapes and burns.

Warnings

When using this product: do not use in the eyes, with deep or puncture wounds, serious burns or animal bites.

Stop using this product:

  • if skin irritation and redness develop
  • if condition persists for more than 72 hours, consult a physician.

For external use only.

Keep this and all drugs out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions Cleanse the affected area according to protocol.

Inactive ingredients water, sodium lauroamphoacetate, cocamidopropyl betaine, glycerin, polysorbate 20, citric acid, quaternium-52, quaternium-15, tetrasodium EDTA

Protocol: Shake well before use. Cleansing: Spray on the affected perineal area and remove with a moist washcloth. Aids in the removal of urine, feces and other foreign material. Ostomy/Incontinence Appliance: To help control odor, spray into appliance before and after use.

Manufactured by: Coloplast A/S
DK-3050 Humlebaek, Denmark
Distributed by: Coloplast Corp.
Minneapolis, MN 55411 U.S.A.
1-800-533-0464 www.us.coloplast.com
Product #1453 ©2009-2, Coloplast Corp.
Made in the U.S.A.

B9-1383

PRINCIPAL DISPLAY PANEL - NET WT. 8 fl. oz. (237mL)

NDC 11701-059-05

Bedside-Care® Perineal Wash

Perineal Skin Cleanser

No-Rinse

Incontinent Cleanser

For Perineal Clean-Up

Coloplast

NET WT. 8 fl. oz. (237mL)

BEDSIDE-CARE PERINEAL WASH  
benzethonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11701-059
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (BENZETHONIUM) BENZETHONIUM CHLORIDE1 mL  in 1 L
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID 
EDETATE SODIUM 
QUATERNIUM-15 
GLYCERIN 
QUATERNIUM-52 
POLYSORBATE 20 
COCAMIDOPROPYL BETAINE 
SODIUM LAUROAMPHOACETATE 
WATER 
Packaging
#Item CodePackage Description
1NDC:11701-059-040.118 L in 1 BOTTLE, SPRAY
2NDC:11701-059-050.237 L in 1 BOTTLE, SPRAY
3NDC:11701-059-093.8 L in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/15/2009
Labeler - Coloplast Manufacturing US, LLC (110326675)
Registrant - Coloplast Corp (847436391)
Establishment
NameAddressID/FEIOperations
Coloplast Manufacturing US, LLC110326675MANUFACTURE

Revised: 06/2011
 
Coloplast Manufacturing US, LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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