GREAT VALUE GREEN APPLE SCENT- chloroxylenol green apple soap 
Sun Products Corporation

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.

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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, FD&C Blue No. 1

Questions? 1-877-505-2267

24 oz frnt bk lbl60 oz frnt lbl60 oz bk lbl

GREAT VALUE GREEN APPLE SCENT 
chloroxylenol green apple soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-034
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)  
WATER (UNII: 059QF0KO0R)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
ALCOHOL (UNII: 3K9958V90M)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63691-034-10709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/30/2016
2NDC:63691-034-301774 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/30/2016
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/30/2016
Labeler - Sun Products Corporation (070931480)

Revised: 3/2017
Document Id: 4a2a28d2-7145-595b-e054-00144ff8d46c
Set id: 4bcc5b97-ef27-4f86-bf3e-bed1511207fc
Version: 4
Effective Time: 20170307
 
Sun Products Corporation