Your browser does not support JavaScript! ANTIBACTERIAL MOIST WIPE (BENZALKONIUM CHLORIDE) SWAB [GREENBRIER INTERNATIONAL, INC.]
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RxNorm Names

ANTIBACTERIAL MOIST WIPE (benzalkonium chloride) swab
[Greenbrier International, Inc.]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL OTC monograph not final
NOTE: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 Label Sections

Active Ingredient

Benzalkonium chloride 0.1%

Purpose

Antibacterial

Use

decreases bacteria on skin

Warnings

For external use only.

Do not use

  • over large areas of the body
  • if you are allergic to any of the ingredients

When using this product

avoid contact with eyes.

In contact occurs, flush thoroughly with water.

Stop use and ask a doctor if

irritation or rash develops and continues for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • for adults and children of 2 years and over
  • children under 2 years ask a doctor before use
  • allow to dry without wiping

Inactive ingredient

Water, Sodium Lauryl sulfate, Fragrance, 2-Bromo-2-Nitropropane-1, 3-Diol, Aloe Barbadensis Leaf Extract, Disodium EDTA, Triethanolamine, Glycerin, Tocopheryl Acetate

Antibacterial Moist Wipes 20 count (33992-2100-0)

DrugFacts

PackageLabel

ANTIBACTERIAL MOIST WIPE  
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:33992-2100
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURYL SULFATE 
BRONOPOL 
ALOE VERA LEAF 
EDETATE DISODIUM 
TROLAMINE 
GLYCERIN 
.ALPHA.-TOCOPHEROL ACETATE 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:33992-2100-080 mL in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/10/2012
Labeler - Greenbrier International, Inc. (610322518)

Revised: 10/2013
 
Greenbrier International, Inc.

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