DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH  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 Foaming Hand Wash
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) • Glycerin • Lauramine Oxide • Cetrimonium Chloride • Cocamidopropyl Betaine • Citric Acid • Sodium Benzoate • Hydroxypropyl Methylcellulose • Parfum (Fragrance) • Zinc Sulfate • Sodium Chloride • Dimethyl Lauramine • Tetrasodium EDTA • Alcohol • Dimethyl Myristamine • CI 42090 (Blue 1) • CI17200 (Red 33)

Distributed by Henkel
Corporation, Rocky Hill, CT 06067

PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label

KILLS 99.99% OF BACTERIA*

#1 DR. RECOMMENDED#

Dial
COMPLETE®

FOAMING
antibacterial
HAND WASH

spring
water®

REFILL
USE ONLY
IN DIAL
COMPLETE®
FOAM PUMP

SKIN
SMART

moisturizing conditioners
gentle cleansers
free from parabens,
phthalates, silicones

52 FL OZ (1.62 QT) 1.53 L REFILL

2632116

PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label
DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH   SPRING WATER
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69560-456
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)  
Lauramine Oxide (UNII: 4F6FC4MI8W)  
Cetrimonium Chloride (UNII: UC9PE95IBP)  
Glycerin (UNII: PDC6A3C0OX)  
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
Anhydrous Citric Acid (UNII: XF417D3PSL)  
Hypromellose, Unspecified (UNII: 3NXW29V3WO)  
Sodium Benzoate (UNII: OJ245FE5EU)  
Zinc Sulfate Heptahydrate (UNII: N57JI2K7WP)  
Edetate Sodium (UNII: MP1J8420LU)  
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:69560-456-021530 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2021
2NDC:69560-456-03946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E05/01/2021
Labeler - MID-CONTINENT PACKAGING, INC. (798250239)

Revised: 12/2021
Document Id: 4e58585e-f0c1-473e-b58f-590429610961
Set id: 52872f6c-5a9c-4da7-b2e9-de22a040bca5
Version: 2
Effective Time: 20211216
 
MID-CONTINENT PACKAGING, INC.