OUR FAMILY DISH AND ANTIBACTERIAL CITRUS BURST SCENT  - triclosan 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

Triclosan 0.10%

Use helps fight germs on hands when used as a hand soap

For external use only

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.  In case of eye contact, rinse thoroughly with water.

Directions wash hands and rinse

Antibacterial hand soap

Inactive ingredients Water, TEA-Dodecylbenzenesulfonate, Sodium Laureth Sulfate, Sodium Methyl 2-Sulfopalmitate, Lauramine Oxide, Sodium Lauryl Sulfate, Alcohol Denat., Disodium 2-Sulfopalmitate, Methyl Palmitate, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, Yellow No. 5, Red No. 33

Questions or comments? 1-800-776-6702

front label

LBLFR

back label

LBLBK

OUR FAMILY DISH AND ANTIBACTERIAL CITRUS BURST SCENT  
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
ALCOHOL (UNII: 3K9958V90M)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T)  
METHYL PALMITATE (UNII: DPY8VCM98I)  
EDETATE SODIUM (UNII: MP1J8420LU)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
SULISOBENZONE (UNII: 1W6L629B4K)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63691-009-10709 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/01/2010
Labeler - Sun Products Corporation (070931480)

Revised: 12/2014
Document Id: a6cce003-e881-4954-9a8c-1f8681b542d9
Set id: 182feec2-e869-40b2-95ff-98e6871f4427
Version: 2
Effective Time: 20141229
 
Sun Products Corporation