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Up (and) Up Green Apple Scent by Sun Products Corporation

Medically reviewed on July 2, 2018

Dosage form: soap
Ingredients: CHLOROXYLENOL 0.3g in 100mL
Labeler: Sun Products Corporation
NDC Code: 63691-029

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

Warnings

For external use only

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.

Purpose

Antibacterial hand soap

Inactive ingredients

Water, Sodium Laureth Sulfate, Sodium Dodecylbenzenesulfonate, Sodium Chloride, Alcohol Denat., Sodium Xylenesulfonate, Soidum Lauryl Sulfate, Tetrasodium EDTA, Benzisothiazolinone, Methylisothiazolinone, Methylchloroisothiazolinone, Fragrance, FD&C Yello No. 5, FD&C Blue No. 1

Questions? 1-800-910-6874

Target 60oz GAAB LDU 690004755_690005736-page-001.jpg
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UP (AND) UP GREEN APPLE SCENT 
chloroxylenol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-029
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 
SODIUM XYLENESULFONATE 
EDETATE SODIUM 
BENZISOTHIAZOLINONE 
WATER 
SODIUM DODECYLBENZENESULFONATE 
SODIUM CHLORIDE 
ALCOHOL 
SODIUM LAURYL SULFATE 
METHYLISOTHIAZOLINONE 
METHYLCHLOROISOTHIAZOLINONE 
FD&C YELLOW NO. 5 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:63691-029-301774 mL in 1 BOTTLE
2NDC:63691-029-10709 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/30/2015
Labeler - Sun Products Corporation (070931480)

 
Sun Products Corporation

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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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