DIAL COMPLETE ALOE- antibacterial hand wash aloe solution DIAL COMPLETE GOLD- antibacterial hand wash gold solution DIAL COMPLETE SPRING WATER- antibacterial hand wash spring water solution DIAL COMPLETE WHITE TEA- antibacterial hand wash white tea solution

Dial Complete BW Apple Blossom by

Drug Labeling and Warnings

Dial Complete BW Apple Blossom by is a Otc medication manufactured, distributed, or labeled by Henkel Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

For Handwashing to decreases bacteria on the skin.

Warnings

For externernal use only.

When Using this Product

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

Stop use and ask 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

• Pump in to hands, wet as needed.
• Later vigorously for at least 15 seconds.
• Wash skin, rinse thoroughly and dry.

Inactive Ingredients

Gold

Aqua (Water, Eau)· Lauramidopropylamine Oxide· Glycerin· Cetrimonium Chloride· Lauramine Oxide· Sodium Chloride·
PEG-120 Methyl Glucose Dioleate · Citric Acid · Sodium Benzoate · Myristamidopropylamlne Oxide · Zinc Sulfate ·
Parfum (Fragrance) Dimethyl Lauramine Tetrasodium EDTA ·Alcohol· Dimethyl Myrlstamine · Cl 19140 (Yellow 5) Cl 14700 (Red 4)

Aloe

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 · Aloe Barbadensis Leaf Juice· Dimethyl Lauramlne · Tetrasodium EDTA ·Alcohol· Dimethyl Myristamine
· Cl 19140 (Yellow 5) · Cl 42090 (Blue 1)

Spring Water

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 · Cl 42090 (Blue 1) · Cl 17200 (Red 33)

White Tea

Aqua (Water, Eau) · Lauramidopropylamine Oxide · Glycerin · Lauramine Oxide · Cetrimonium Chloride·
Sodium Chloride· PEG-120 Methyl Glucose Dioleate · Citric Acid· Sodium Benzoate · Myristamidopropylam!ne Oxide·
Parfum (Fragrance)· Zinc Sulfate· Dimethyl Lauramine Tetrasodium EDTA · Alcohol· Camellia Sinensis Leaf Extract·
Dimethyl Myristamine · Cl 42090 (Blue 1) · Cl 17200 (Red 33)

Questions

call 1-800-258-DIAL(3425)

Legal Entity

www.dialsoap.com

henkel Bean Logo

R,TM,c2019 Distributed by

Henkel Corporation,Rocky Hill, CT 06067

^Encountered in household settings

#Antibacterial Hand Soap

INDICATIONS & USAGE

For handwasing to decrease bacteria on the skin.

Topical Liquid

Liquid Hand Soap

Front and the back of the pack

INGREDIENTS AND APPEARANCE

DIAL COMPLETE ALOE 
antibacterial hand wash aloe solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-146
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE SODIUM (UNII: MP1J8420LU)	0.02 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	90.27 mL  in 100 mL
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)
ZINC SULFATE (UNII: 89DS0H96TB)	0.05 mL  in 100 mL
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHYL MYRISTAMINE (UNII: 5E4O85D8T2)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.4 mL  in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 mL  in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-146-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC: 54340-146-02	277 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
3	NDC: 54340-146-03	1180 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

DIAL COMPLETE GOLD 
antibacterial hand wash gold solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-143
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE SODIUM (UNII: MP1J8420LU)	0.02 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	90.43 mL  in 100 mL
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)	0.005624 mL  in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)
ZINC SULFATE (UNII: 89DS0H96TB)	0.05 mL  in 100 mL
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHYL MYRISTAMINE (UNII: 5E4O85D8T2)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.4 mL  in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 mL  in 100 mL
FD&C RED NO. 4 FREE ACID (UNII: WJE3T5596E)	0.000288 mL  in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.9503 mL  in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-143-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC: 54340-143-02	1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

DIAL COMPLETE SPRING WATER 
antibacterial hand wash spring water solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-142
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)	90.34 mL  in 100 mL
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)
ZINC SULFATE (UNII: 89DS0H96TB)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHYL MYRISTAMINE (UNII: 5E4O85D8T2)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ALCOHOL (UNII: 3K9958V90M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-142-02	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC: 54340-142-04	946 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
3	NDC: 54340-142-05	1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

DIAL COMPLETE WHITE TEA 
antibacterial hand wash white tea solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-145
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)	90.46 mL  in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)
ZINC SULFATE (UNII: 89DS0H96TB)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHYL MYRISTAMINE (UNII: 5E4O85D8T2)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ALCOHOL (UNII: 3K9958V90M)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-145-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - Henkel Corporation (080887708)

Registrant - Henkel Corporation (080887708)