![UP (AND) UP GREEN APPLE SCENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]](https://medic.hrt.org//dailymed/images/25692dd8-1a8d-48db-b6bd-b46c58ce52fb/target_upup_690001672_fr.jpg)
![UP (AND) UP GREEN APPLE SCENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]](https://medic.hrt.org//dailymed/images/25692dd8-1a8d-48db-b6bd-b46c58ce52fb/target_upup_690001779_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, Yellow No. 5, Blue No.1
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
UP (AND) UP GREEN APPLE SCENT
triclosan soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63691-019 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 DODECYLBENZENESULFONATE (UNII: 554127163Y) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) ALCOHOL (UNII: 3K9958V90M) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T) METHYL PALMITATE (UNII: DPY8VCM98I) SODIUM METABISULFITE (UNII: 4VON5FNS3C) EDETATE SODIUM (UNII: MP1J8420LU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) SULISOBENZONE (UNII: 1W6L629B4K) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63691-019-10 709 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/01/2011 Labeler - Sun Products Corporation (070931480)
