CORALITE ANTIBACTERIAL MOIST- benzalkonium chloride solution 
United Exchange Corp.

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.

----------

Coralite Antibacterial Moisturizing Pouch Wipe, 30ct 83103

Drug Facts


Active Ingredient                                                                                      Purpose

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

Uses

Warnings

For external use only

When using this product avoid contact with the eyes, if contact occurs rinse thoroughly with water.

Stop use and ask a doctor if

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

Directions

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

Distributed by:

UNITED EXCHANGE CORP.

17211 Valley View Ave.

Cerritos, CA 90703

MADE IN CHINA

image description

CORALITE ANTIBACTERIAL MOIST 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-831
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.115 g
Inactive Ingredients
Ingredient NameStrength
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)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65923-831-3030 in 1 POUCH; Type 0: Not a Combination Product09/26/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/26/2013
Labeler - United Exchange Corp. (840130579)

Revised: 5/2023
Document Id: fae29043-efde-429a-e053-6294a90acb24
Set id: 6245a83f-5c81-4ae6-bc6e-adfc46c37003
Version: 7
Effective Time: 20230504
 
United Exchange Corp.