Label: DIAL WHITE TEA AND VITAMIN E ANTIBACTERIAL HAND SOAP- triclosan solution
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Contains inactivated NDC Code(s)
NDC Code(s): 54340-802-01, 54340-802-02, 54340-802-03 - Packager: The Dial Corporation
- 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 February 23, 2011
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Water, Sodium Laureth Sulfate, Decyl Glucoside, Cocamidopropyl Betaine, Sodium Chloride, Cocamide MEA, Fragrance, PEG-120 Methyl Glucose Dioleate, PEG-18 Glyceryl Oleate/Cocoate, Propylene Glycol, Camellia Sinensis Leaf Extract, Tocopheryl Acetate, Polyquaternium-7, DMDM Hydantoin, Tetrasodium EDTA, Citric Acid, Ext. Violet 2.
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INGREDIENTS AND APPEARANCE
DIAL WHITE TEA AND VITAMIN E ANTIBACTERIAL HAND SOAP
triclosan solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-802 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan 0.15 mL in 1000 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM CHLORIDE (UNII: 451W47IQ8X) COCO MONOETHANOLAMIDE (UNII: C80684146D) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) POLYETHYLENE GLYCOL 900 (UNII: UEP843BRCQ) GLYCERYL MONOOLEATE (UNII: 4PC054V79P) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ACETATE ION (UNII: 569DQM74SC) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y) DMDM HYDANTOIN (UNII: BYR0546TOW) EDETATE SODIUM (UNII: MP1J8420LU) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-802-01 221 mL in 1 BOTTLE, PUMP 2 NDC:54340-802-02 277 mL in 1 BOTTLE, PUMP 3 NDC:54340-802-03 1540 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/01/2011 Labeler - The Dial Corporation (070252531) Establishment Name Address ID/FEI Business Operations The Dial Corporation West Hazelton 825091622 manufacture