Label: SCOTT CLEAR ANTIBACTERIAL SKIN CLEANSER- triclosan solution
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Contains inactivated NDC Code(s)
NDC Code(s): 55118-205-05, 55118-205-08, 55118-205-10 - Packager: Kimberly-Clark 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 October 7, 2014
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- Active Ingredient
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- Inactive Ingredients
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 500 mL Carton
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INGREDIENTS AND APPEARANCE
SCOTT CLEAR ANTIBACTERIAL SKIN CLEANSER
triclosan solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55118-205 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan 0.25 g in 100 mL Inactive Ingredients Ingredient Name Strength Sodium Laureth-3 Sulfate (UNII: BPV390UAP0) Sodium Chloride (UNII: 451W47IQ8X) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) Coco Diethanolamide (UNII: 92005F972D) Glycerin (UNII: PDC6A3C0OX) Propylene Glycol (UNII: 6DC9Q167V3) Panthenol (UNII: WV9CM0O67Z) Aloe Vera Leaf (UNII: ZY81Z83H0X) Citric Acid Monohydrate (UNII: 2968PHW8QP) Methylchloroisothiazolinone (UNII: DEL7T5QRPN) Methylisothiazolinone (UNII: 229D0E1QFA) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55118-205-05 500 mL in 1 BAG; Type 0: Not a Combination Product 2 NDC:55118-205-08 800 mL in 1 BAG; Type 0: Not a Combination Product 3 NDC:55118-205-10 1000 mL in 1 BAG; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 03/01/2012 Labeler - Kimberly-Clark Corporation (006072136)