CORALITE ANTIBACTERIAL MOIST- benzalkonium chloride solution 
United Exchange Corp.

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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

adults and children 12 years and overRub on hands for 30 seconds and allow skin to dry without wiping
children under 2 yearsask a doctor before use

Inactive ingredients

aqua, aloe barbadensis leaf juice powder, 2-Bromo-2-Nitropropane-1,3-Diol, Chamomilla Recutita Flower Extract, Citric Acid, Iodopropynl butylcarbamate, 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

83103

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
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BRONOPOL (UNII: 6PU1E16C9W)  
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)  
MATRICARIA CHAMOMILLA ROOT (UNII: BTG5H50X7F)  
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 DrugM00309/26/2013
Labeler - United Exchange Corp. (840130579)

Revised: 7/2024
Document Id: 1d88152e-066a-7c17-e063-6394a90a1f0c
Set id: 6245a83f-5c81-4ae6-bc6e-adfc46c37003
Version: 8
Effective Time: 20240718
 
United Exchange Corp.