Label: BENZETHONIUM CHLORIDE SOLUTION- dial complete clean citrus foaming antibacterial hand wash solution
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Contains inactivated NDC Code(s)
NDC Code(s): 54340-252-01 - Packager: The Dial Corporation, A Henkel Company
- 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 17, 2014
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- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- PURPOSE
- WARNINGS
- WHEN USING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- INSTRUCTIONS FOR USE
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BENZETHONIUM CHLORIDE SOLUTION
dial complete clean citrus foaming antibacterial hand wash solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-252 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE .2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-252-01 221 mL in 1 BOTTLE, PUMP 01/05/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/05/2015 Labeler - The Dial Corporation, A Henkel Company (070252531) Establishment Name Address ID/FEI Business Operations The Dial Corporation 825091622 manufacture(54340-252)