BENZETHONIUM CHLORIDE SOLUTION- dial spring water antibacterial hand soap solution

Benzethonium Chloride Solution by

Drug Labeling and Warnings

Benzethonium Chloride Solution by is a Otc medication manufactured, distributed, or labeled by The Dial Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

ACTIVE INGREDIENT

Benzethonium Chloride 0.10%

PURPOSE

Antibacterial

PURPOSE

Uses - For handwashing to decrease bacteria on the skin

WARNINGS

For external use only

WHEN USING

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

ASK DOCTOR

Stop use and ask a doctor if irritation and redness develops

KEEP OUT OF REACH OF CHILDREN

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

INSTRUCTIONS FOR USE

Directions

• pump into hands, wet as needed
• lather vigorously for at least 15 seconds
• wash skin, rinse thoroughly and dry

INACTIVE INGREDIENT

Inactive Ingredients: Water, Centrimonium Chloride, Glycerin, Lauramine Oxide, Lauramidopropylamine Oxide, Sodium Chloride, Fragrance, PEG-120 Methyl Glucose Dioleate, Cocamide MEA, Citric Acid, Sodium Benzoate, Tetrasodium EDTA, Blue 1, Red 33

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* Encountered in household settings

QUESTIONS

Questions? 1-800-258-DIAL (3425)

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Visit our web site at www.dialsoap.com

© 2013 THE DIAL CORPORATION, A (HENKEL) COMPANY SCOTTSDALE, AZ 85255

MADE IN USA

The distinctive design and elements of this package are proprietary and owned by The Dial Corporation, A Henkel Company.

DOSAGE & ADMINISTRATION

Topical Liquid

INDICATIONS & USAGE

For handwashing to decrease bacteria on skin

PRINCIPAL DISPLAY PANEL

KILLS 99.9% OF GERMS*

New Active!

TOTAL CLEAN FORMULA

Refill ONLY with Dial® Total Clean Formula

Dial Spring Water® Hand Soap with Moisturizer

Antibacterial

7.5 FL OZ (221 mL)

INGREDIENTS AND APPEARANCE

BENZETHONIUM CHLORIDE SOLUTION 
dial spring water antibacterial hand soap solution

Product 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)