Label: TORK PREMIUM- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 49351-015-01, 49351-015-02 - Packager: SCA Tissue North America
- Category: HUMAN OTC DRUG LABEL
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 March 29, 2010
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
- Directions
- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 800 mL Carton
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INGREDIENTS AND APPEARANCE
TORK PREMIUM
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49351-015 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Propylene Glycol (UNII: 6DC9Q167V3) Lactic Acid (UNII: 33X04XA5AT) Sodium Laureth Sulfate (UNII: BPV390UAP0) Sodium Hydroxide (UNII: 55X04QC32I) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) Benzyl Alcohol (UNII: LKG8494WBH) Methylchloroisothiazolinone (UNII: DEL7T5QRPN) Methylisothiazolinone (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49351-015-01 1 in 1 BOX 1 800 mL in 1 BAG 2 NDC:49351-015-02 4 in 1 CARTON 2 1100 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 03/03/2010 Labeler - SCA Tissue North America (005694349) Registrant - Rubbermaid Commercial Products LLC (049924368)