Label: BENZETHONIUM CHLORIDE SOLUTION- dial spring water antibacterial hand soap solution
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Contains inactivated NDC Code(s)
NDC Code(s): 54340-242-01, 54340-242-02, 54340-242-03, 54340-242-04, view more54340-242-05 - Packager: The Dial 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 November 25, 2014
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- 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 spring water antibacterial hand soap solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-242 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE .1 g in 100 mL Inactive Ingredients Ingredient Name Strength LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) GLYCERIN (UNII: PDC6A3C0OX) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM BENZOATE (UNII: OJ245FE5EU) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) SODIUM CHLORIDE (UNII: 451W47IQ8X) COCO MONOETHANOLAMIDE (UNII: C80684146D) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-242-01 162 mL in 1 BOTTLE, PUMP 01/05/2015 2 NDC:54340-242-02 221 mL in 1 BOTTLE, PUMP 01/05/2015 3 NDC:54340-242-03 277 mL in 1 BOTTLE, PUMP 01/05/2015 4 NDC:54340-242-04 946 mL in 1 BOTTLE, DISPENSING 01/05/2015 5 NDC:54340-242-05 1530 mL in 1 BOTTLE, DISPENSING 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 (070252531) Establishment Name Address ID/FEI Business Operations The Dial Corporation 825091622 manufacture(54340-242)