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Wegmans Ultra Dishwashing Liquid Orange Scent

Dosage form: soap
Ingredients: CHLOROXYLENOL 0.3g in 100mL
Labeler: Sun Products Corporation
NDC Code: 63691-035

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.

Active ingredient

Chloroxylenol 0.30%

Use for handwashing to decrease bacteria on the skin

For external use only

Keep out of reach of children. In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

Directions wet hands and forearms. Apply 5 mL or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

Antibacterial hand soap

Inactive ingredients Water, Sodium Laureth Sulfate, Sodium Dodecylbenzenesulfonate, Sodium Chloride, Alcohol Denat., Sodium Xylenesulfonate, Sodium Lauryl Sulfate, Tetrasodium EDTA, Benzisothiazolinone, Methylisothiazolinone, Methylchloroisothiazolinone, Fragrance, FD&C Yellow No. 5, D&C Red No. 33

Questions? 1-800-Wegmans (934-6267) Ext 5920

WEGMANS ULTRA DISHWASHING LIQUID ORANGE SCENT 
dishwashing liquid orange scent soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-035
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM LAURETH SULFATE 
METHYLISOTHIAZOLINONE 
FD&C YELLOW NO. 5 
SODIUM CHLORIDE 
WATER 
ALCOHOL 
SODIUM LAURYL SULFATE 
SODIUM XYLENESULFONATE 
METHYLCHLOROISOTHIAZOLINONE 
SODIUM DODECYLBENZENESULFONATE 
D&C RED NO. 33 
EDETATE SODIUM 
BENZISOTHIAZOLINONE 
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:63691-035-10709 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/31/2016
Labeler - Sun Products Corporation (070931480)

 
Sun Products Corporation

Medically reviewed on Mar 13, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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