CORALITE ANTIBACTERIAL MOIST- benzalkonium chloride solution

Coralite Antibacterial Moist by

Drug Labeling and Warnings

Coralite Antibacterial Moist by is a Otc medication manufactured, distributed, or labeled by United Exchange Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient                                                                                      Purpose

Benzalkonium Chloride 0.115%............................................................ Antibacterial

PURPOSE

Uses

• Decreases bacteria on skin and surfaces

WARNINGS

Warnings

For external use only

STOP USE

Stop use and ask a doctor if

• Irritation or rash develops and persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Directions

• Peel back seal using tab. Do not pull seal all the way off. Pull sheet from center and remove as needed. Reseal pouch by pressing seal back down to retain moisture after each use.
• Apply thoroughly to hands and face as desired and allow to dry without wiping.
• Dispose of wipe in the proper container. Do not flush down the toilet.

INACTIVE INGREDIENT

Inactive ingredients

2-Bromo-2-Nitropropane-1,3-Diol,3-Iodo-2-propynyl Butyl Carbamate, Aloe Gel Powder 100:1, Aqua, Chamomilla Recutita Flower Extract (Propylene Glycol, Aqua), Citric Acid, Lauryl Glucoside, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Sodium Citrate, Terasodium EDTA

DOSAGE & ADMINISTRATION

Distributed by:

UNITED EXCHANGE CORP.

17211 Valley View Ave.

Cerritos, CA 90703

MADE IN CHINA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CORALITE ANTIBACTERIAL MOIST 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-831
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.115 g

Inactive Ingredients
Ingredient Name	Strength
BRONOPOL (UNII: 6PU1E16C9W)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
CITRIC ACID ACETATE (UNII: DSO12WL7AU)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
EDETATE SODIUM (UNII: MP1J8420LU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-831-30	30 in 1 POUCH; Type 0: Not a Combination Product	09/26/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/26/2013

Labeler - United Exchange Corp. (840130579)