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Coralite Antibacterial Moist

Dosage form: solution
Ingredients: BENZALKONIUM CHLORIDE 0.115g
Labeler: United Exchange Corp.
NDC Code: 65923-831

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.

Drug Facts


Active Ingredient                                                                                      Purpose

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

Uses

  • Decreases bacteria on skin and surfaces

Warnings

For external use only

Stop use and ask a doctor if

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

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

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 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

CORALITE ANTIBACTERIAL MOIST 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-831
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.115 g
Inactive Ingredients
Ingredient NameStrength
BRONOPOL 
IODOPROPYNYL BUTYLCARBAMATE 
CITRIC ACID ACETATE 
LAURYL GLUCOSIDE 
PHENOXYETHANOL 
POLYSORBATE 20 
PROPYLENE GLYCOL 
SODIUM CITRATE 
EDETATE SODIUM 
Packaging
#Item CodePackage Description
1NDC:65923-831-3030 SOLUTION in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/26/2013
Labeler - United Exchange Corp. (840130579)

Revised: 09/2013
 
United Exchange Corp.

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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