DIAL PROFESSIONAL ANTIBACTERIAL DEFENSE SPRING WATER- benzalkonium chloride solution DIAL PROFESSIONAL ANTIBACTERIAL AND SENSITIVE FRAGRANCE FREE- benzalkonium chloride solution DIAL PROFESSIONAL ANTIBACTERIAL DEFENSE GOLD- benzalkonium chloride solution

Dial Professional Antibacterial Defense Gold by

Drug Labeling and Warnings

Dial Professional Antibacterial Defense Gold 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 external 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 into hands, wet as needed.
• Lather vigorously for at least 30 seconds.
• Wash skin, rinse thoroughly and dry.

Inactive Ingredients

Variant Gold:

Inactive ingredients: Aqua (Water, Eau) · Sodium Chloride · Lauramidopropylamine Oxide · Glycerin · Cetrimonium Chloride · Lauramine Oxide · PEG-120 Methyl Glucose Dioleate · Citric Acid · Sodium Benzoate · Myristamidopropylamine Oxide · Parfum (Fragrance) · Aloe Barbadensis Leaf Juice · Zinc Sulfate · Trisodium Ethylenediamine Disuccinate · Dimethyl Lauramine. Alcohol. CI 19140 (yellow 5). CI 14700 (Red 4)

Variant AB Fragrance Free:

Inactive ingredients: Aqua (Water, Eau) · Sodium Chloride · Lauramidopropylamine Oxide · Glycerin · Cetrimonium Chloride · Lauramine Oxide ·
PEG-120 Methyl Glucose Dioleate · Citric Acid · Sodium Benzoate · Myristamidopropylamine Oxide · Aloe Barbadensis Leaf Juice · Zinc Sulfate · Trisodium Ethylenediamine Disuccinate · Dimethyl Lauramine · Alcohol

Variant Spring Water:

Inactive ingredients: Aqua (Water, Eau) · Sodium Chloride · Lauramidopropylamine Oxide · Glycerin · Cetrimonium Chloride · Lauramine Oxide ·
PEG-120 Methyl Glucose Dioleate · Citric Acid · Sodium Benzoate · Parfum (Fragrance) · Myristamidopropylamine Oxide · Aloe Barbadensis Leaf Juice · Zinc Sulfate · Trisodium Ethylenediamine Disuccinate · Dimethyl Lauramine · Alcohol · CI 42090 (Blue 1) · CI 17200 (Red 33)

Questions

Questions? 1-877-777-3277

Legal Entity

henkel Bean Logo

R,TM,c2024 Distributed by

Henkel Corporation,Rocky Hill, CT 06067

www.dialsprofessional.com

^Encountered in household settings

#Antibacterial Hand Soap

Indications & Usage

For handwasing to decrease bacteria on the skin.

Topical Liquid

Liquid Hand Soap

Principal Display Panel

INGREDIENTS AND APPEARANCE

DIAL PROFESSIONAL ANTIBACTERIAL DEFENSE SPRING WATER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-121
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
ZINC SULFATE (UNII: 89DS0H96TB)	0.05 g  in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g  in 100 mL
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)	1.635 g  in 100 mL
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)	0.19 g  in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g  in 100 mL
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0162 g  in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.975 g  in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.575 g  in 100 mL
WATER (UNII: 059QF0KO0R)	89.65 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g  in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	1.5 g  in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.4 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.5 g  in 100 mL
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)	0.75 g  in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	2.2 g  in 100 mL
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)	0.000051 g  in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.000017 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-121-02	4 in 1 CARTON	01/01/2024
1	NDC: 54340-121-01	3785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2024

DIAL PROFESSIONAL ANTIBACTERIAL AND SENSITIVE FRAGRANCE FREE 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-309
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
ZINC SULFATE (UNII: 89DS0H96TB)	0.05 g  in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g  in 100 mL
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)	1.635 g  in 100 mL
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)	0.19 g  in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g  in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.975 g  in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.575 g  in 100 mL
WATER (UNII: 059QF0KO0R)	89.727 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g  in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	1.5 g  in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.4 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.5 g  in 100 mL
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)	0.75 g  in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	2.4 g  in 100 mL
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0162 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-309-04	4 in 1 CARTON	01/01/2024
1	NDC: 54340-309-03	3785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
2	NDC: 54340-309-02	8 in 1 CARTON	01/01/2024
2	NDC: 54340-309-01	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
3	NDC: 54340-309-06	12 in 1 CARTON	01/01/2024
3	NDC: 54340-309-05	325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2024

DIAL PROFESSIONAL ANTIBACTERIAL DEFENSE GOLD 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-302
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
ZINC SULFATE (UNII: 89DS0H96TB)	0.05 g  in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g  in 100 mL
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)	1.635 g  in 100 mL
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)	0.19 g  in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g  in 100 mL
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0162 g  in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.975 g  in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.575 g  in 100 mL
WATER (UNII: 059QF0KO0R)	89.8 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g  in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	1.5 g  in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.4 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.5 g  in 100 mL
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)	0.75 g  in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	2.2 g  in 100 mL
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)	0.0056 g  in 100 mL
FD&C RED NO. 4 (UNII: X3W0AM1JLX)	0.00029 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-302-02	12 in 1 CARTON	01/01/2024
1	NDC: 54340-302-01	325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 54340-302-06	6 in 1 CARTON	01/01/2024
2	NDC: 54340-302-05	443 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
3	NDC: 54340-302-04	4 in 1 CARTON	01/01/2024
3		3785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
4	NDC: 54340-302-03	8 in 1 CARTON	01/01/2024
4		1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
5	NDC: 54340-302-08	144 in 1 CARTON	01/01/2024
5	NDC: 54340-302-07	59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
6	NDC: 54340-302-09	3785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/30/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2024

Labeler - Henkel Corporation (080887708)