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Great Value Orange Scent

Medically reviewed on March 7, 2017

Dosage form: soap
Ingredients: CHLOROXYLENOL 0.3g in 100mL
Labeler: Sun Products Corporation
NDC Code: 63691-033

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 helps fight germs on hands when used as a hand soap

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.

Dishwashing Liquid and 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? 1-877-505-2267

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GREAT VALUE ORANGE SCENT 
orange chloroxylenol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-033
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
METHYLCHLOROISOTHIAZOLINONE 
FD&C YELLOW NO. 5 
SODIUM CHLORIDE 
WATER 
SODIUM LAURETH SULFATE 
D&C RED NO. 33 
EDETATE SODIUM 
ALCOHOL 
BENZISOTHIAZOLINONE 
SODIUM XYLENESULFONATE 
SODIUM LAURYL SULFATE 
METHYLISOTHIAZOLINONE 
SODIUM DODECYLBENZENESULFONATE 
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:63691-033-10709 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/01/2016
Labeler - Sun Products Corporation (070931480)

 
Sun Products Corporation

Further information

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

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