BerbereX Wound Cleanser

Dosage form: liquid
Ingredients: ALLANTOIN 5g in 1000mL, BENZETHONIUM CHLORIDE 1g in 1000mL
Labeler: Cosco International, Inc.
NDC code: 52261-0500

Medically reviewed by Drugs.com. Last updated on Jan 17, 2024.

Drug Facts

Active Ingredient/Purpose

Allantoin 0.5%........................Skin Protectant

Benzethonium Chloride............Antiseptic

Uses

helps protect skin and supports healing of minor cuts, scrapes, burns and wounds, including pressure sores, diabetic ulcers, cracked skin and lips
topical antiseptic to help decrease the risk of skin infections

Warnings For external use only.

Do not use

in large quantities, particularly over raw surfaces or blistered areas

Ask doctor before use if you have

deep or puncture wounds
animal bites
serious burns

Stop use and ask doctor if

condition worsens
symptons persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately

Directions:

Adults and children 2 years of age and older:

use to clean minor cut, scrapes, and burns by thoroughly flushing the affected area
let air dry
cover with adhesive bandage or sterile gauze
apply a small amount of this product on the area 1 to 3 times daily

Children under 2 years of age: do not use, consult a doctor

Inactive ingredients:

Aloe barbadensis Mill, Ethanol, Hydrastis canadensis L., Hydrogen Peroxide, Panax quinquefolis L., Water

BERBEREX WOUND CLEANSER
benzethonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:52261-0500
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (ALLANTOIN)	ALLANTOIN	5 g in 1000 mL
BENZETHONIUM CHLORIDE (BENZETHONIUM)	BENZETHONIUM CHLORIDE	1 g in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
water
ALCOHOL
ALOE VERA WHOLE
HYDRASTIS CANADENSIS WHOLE
PANAX QUINQUEFOLIUS WHOLE
hydrogen peroxide

Packaging
#	Item Code	Package Description
1	NDC:52261-0500-1	118 mL in 1 BOTTLE, SPRAY
2	NDC:52261-0500-2	237 mL in 1 BOTTLE, SPRAY
3	NDC:52261-0500-3	473 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/17/2015

Labeler - Cosco International, Inc. (016433141)

Registrant - Cosco International, Inc. (016433141)

Establishment
Name	Address	ID/FEI	Operations
Cosco International, Inc.		016433141	manufacture(52261-0500), label(52261-0500), pack(52261-0500)

Revised: 01/2020

Document Id: af7d3c7f-8c60-405d-9d52-6c040ac81e3a

Set id: 08b28f52-21fc-4694-a163-91c8193b4008

Version: 5

Effective Time: 20200127

Cosco International, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer