Drug Facts

DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASHHOLIDAY LINE HOLIDAY LINE HOLIDAY LINE- triclosan solution
The Dial Corporation

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.

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Drug Facts

Active Ingredient - TRICLOSAN 0.46%

Antibacterial

For hand washing to decrease bacteria on the skin

For external use only.

Stop use and ask a doctor if irritation and redness develops.

When using this product avoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor irritation and redness develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions: Pump into dry hands. Lather vigorously for 15 seconds. Rinse and dry thoroughly.

Inactive Ingredients: Water, Sodium Xylenesulfonate, Dipropylene Glycol, Glycerin, Sodium PCA, Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Polyquaternium-10, Fragrance, Disodium Phosphate, Cetyl Alcohol, Aloe Barbadensis Leaf juice, Citric Acid, Methylparaben, Propylparaben, Red 4, Yellow 5

Questions? 1-800-258-DIAL

Label image

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DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASHHOLIDAY LINE HOLIDAY LINE HOLIDAY LINE
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-814
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	4.6 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
POLYQUATERNIUM-10 (400 MPA.S AT 2%) (UNII: HB1401PQFS)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
CETYL ALCOHOL (UNII: 936JST6JCN)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54340-814-01	221 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	02/15/2012

Labeler - The Dial Corporation (070252531)

Name	Address	ID/FEI	Business Operations
Establishment
The Dial Corporation, West Hazelton		825091622	manufacture(54340-814)