DIAL COMPLETE ANTIBACTERIAL HAND  SPRING WATER- benzalkonium chloride solution 
MID-CONTINENT PACKAGING, INC.

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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Dial Complete® Antibacterial Liquid Hand Soap
Spring Water®

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

Warnings

For external use only

When using this product

  • Avoid contact with eyes. In case of eye contact, flush with water.

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

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

Directions

Inactive ingredients

Aqua (Water, Eau) • Lauramidopropylamine Oxide • Glycerin • Cetrimonium Chloride • Lauramine Oxide • Sodium Chloride • PEG-120 Methyl Glucose Dioleate • Citric Acid • Sodium Benzoate • Myristamidopropylamine Oxide • Parfum (Fragrance) • Zinc Sulfate • Dimethyl Lauramine • Tetrasodium EDTA • Alcohol • Dimethyl Myristamine • CI 42090 (Blue 1) • CI 17200 (Red 33)

Questions?

1-800-258-DIAL (3425)

Distributed by
Henkel Corporation,
Rocky Hill, CT 06067

PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label

KILLS 99.9% OF BACTERIA*

NEW
LOOK!

Dial
COMPLETE®

LIQUID
antibacterial
Hand Soap

SPRING
WATER®

52 FL OZ (1.62 QT) 1.53 L

2370134

PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label
DIAL COMPLETE ANTIBACTERIAL HAND   SPRING WATER
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69560-234
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Lauramidopropylamine Oxide (UNII: I6KX160QTV)  
Lauramine Oxide (UNII: 4F6FC4MI8W)  
Cetrimonium Chloride (UNII: UC9PE95IBP)  
GLYCERIN (UNII: PDC6A3C0OX)  
Sodium Chloride (UNII: 451W47IQ8X)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Sodium Benzoate (UNII: OJ245FE5EU)  
Edetate Sodium (UNII: MP1J8420LU)  
Myristamidopropylamine Oxide (UNII: 3HSF539C9T)  
Zinc Sulfate Heptahydrate (UNII: N57JI2K7WP)  
Dimethyl Lauramine (UNII: 6V2OM30I1Z)  
Alcohol (UNII: 3K9958V90M)  
Dimethyl Myristamine (UNII: 5E4O85D8T2)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Product Characteristics
ColorBLUEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69560-234-021530 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/05/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E05/05/2021
Labeler - MID-CONTINENT PACKAGING, INC. (798250239)

Revised: 4/2021
Document Id: 0e5de26c-4336-4e49-89c7-38a694dd43e9
Set id: c55888fc-c2ff-4d29-ba3e-2ad36c87832e
Version: 1
Effective Time: 20210426
 
MID-CONTINENT PACKAGING, INC.