MY ESSENTIALS CITRUS 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, Sodium Dodecylbenzenesulfonate, Palm Kernelamide DEA, Sodium Methyl 2-Sulfopalmitate, Urea, Sodium Chloride, Disodium 2-Sulfopalmitate, Methyl Palmitate, Fragrance, Sodium Citrate, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, D&C Orange No. 4

Questions? 1-866-322-2439

front label

LBLFR

back label

LBLBK

MY ESSENTIALS CITRUS SCENT  
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-022
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)  
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
UREA (UNII: 8W8T17847W)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T)  
METHYL PALMITATE (UNII: DPY8VCM98I)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
EDETATE SODIUM (UNII: MP1J8420LU)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
SULISOBENZONE (UNII: 1W6L629B4K)  
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63691-022-04739 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/01/2014
Labeler - Sun Products Corporation (070931480)

Revised: 12/2014
Document Id: 17a4893b-4d0a-45c5-b7ed-5bb93393da8a
Set id: ac232de0-aee2-4774-a1e9-88ec5760fe7a
Version: 1
Effective Time: 20141230
 
Sun Products Corporation