![EXCHANGE SELECT ULTRA CITRUS SCENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]](https://medic.hrt.org//dailymed/images/b5c7b438-6472-41e3-872a-d0287737ea1f/exchange_select_690002192_bk.jpg)
![EXCHANGE SELECT ULTRA CITRUS SCENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]](https://medic.hrt.org//dailymed/images/b5c7b438-6472-41e3-872a-d0287737ea1f/exchange_select_690002193_fr.jpg)
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ACTIVE INGREDIENT
Active ingredient
Triclosan 0.10%
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.
Inactive ingredients Water, Sodium Dodecylbenzenesulfonate, Sodium Laureth Sulfate, Sodium Methyl 2-Sulfopalmitate, Magnesium Sulfate, Sodium Xylenesulfonate, Alcohol Denat., Fragrance, Disodium 2-Sulfopalmitate, Methyl Palmitate, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, D&C Orange No. 4, Sodium Citrate
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INGREDIENTS AND APPEARANCE
EXCHANGE SELECT ULTRA CITRUS SCENT
triclosan soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63691-024 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) MAGNESIUM SULFATE (UNII: DE08037SAB) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) ALCOHOL (UNII: 3K9958V90M) DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T) METHYL PALMITATE (UNII: DPY8VCM98I) EDETATE SODIUM (UNII: MP1J8420LU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) SULISOBENZONE (UNII: 1W6L629B4K) D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63691-024-12 591 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 07/01/2014 Labeler - Sun Products Corporation (070931480) Registrant - Military Exchange (827856670) Establishment Name Address ID/FEI Business Operations Sun Products Corporation - Salt Lake City 096752865 manufacture(63691-024) Establishment Name Address ID/FEI Business Operations Sun Products Corporation - Bowling Green 809709314 manufacture(63691-024)
