Label: UP (AND) UP GREEN APPLE SCENT- triclosan soap
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Contains inactivated NDC Code(s)
NDC Code(s): 63691-019-10 - Packager: Sun Products Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated December 23, 2015
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- Official Label (Printer Friendly)
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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)
