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Ultra So-Soft Dish Detergent

Medically reviewed on June 29, 2018

Dosage form: soap
Ingredients: CHLOROXYLENOL 0.3g in 100mL
Labeler: Sun Products Corporation
NDC Code: 63691-028

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.

Dish Detergent Concentrated

Dish Detergent Concentrated and Antibacterial Hand Soap

Active Ingredient

Chloroxylenol 0.30%

Purpose

Antibacterial hand soap

Use

for handwashing to decrease bacteria on the skin

Warnings

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 hand and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

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

Ultra so soft AB hand soap-page-001.jpg

ULTRA SO-SOFT DISH DETERGENT 
chloroxylenol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-028
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL 
WATER 
SODIUM CHLORIDE 
SODIUM XYLENESULFONATE 
SODIUM LAURYL SULFATE 
EDETATE SODIUM 
METHYLCHLOROISOTHIAZOLINONE 
BENZISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
SODIUM LAURETH SULFATE 
SODIUM DODECYLBENZENESULFONATE 
FD&C YELLOW NO. 5 
D&C RED NO. 33 
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:63691-028-10709 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/30/2016
Labeler - Sun Products Corporation (070931480)
Registrant - Wakefern (006972418)

 
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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