![WEGMANS ORANGE SCENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]](https://medic.hrt.org//dailymed/images/ba54aab6-88a2-4886-a33f-a67d3a4a4631/wegmans_690002282_fr.jpg)
![WEGMANS ORANGE SCENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]](https://medic.hrt.org//dailymed/images/ba54aab6-88a2-4886-a33f-a67d3a4a4631/wegmans_690002914_bk.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, Urea, Sodium Laureth Sulfate, Sodium Dodecylbenzenesulfonate, Alcohol Denat., Lauramine Oxide, Magnesium Chloride, Sodium Methyl 2-Sulfopalmitate, Fragrance, Sodium Metabisulfite, Disodium 2-Sulfopalmitate, Methyl Palmitate, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, FD&C Yellow No. 5, D&C Red No. 33
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INGREDIENTS AND APPEARANCE
WEGMANS ORANGE SCENT
triclosan soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63691-026 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) UREA (UNII: 8W8T17847W) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y) ALCOHOL (UNII: 3K9958V90M) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) SODIUM METABISULFITE (UNII: 4VON5FNS3C) 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:63691-026-10 709 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)
