Drug Facts

30 Spring Water

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

Fresh Lavender

Coconut Water

Inactive ingredients: Aqua (Water, Eau) · Glycerin · Cetrimonium Chloride · Lauramine Oxide · Cocamidopropyl Betaine · Sodium Benzoate · Parfum (Fragrance) · Citric Acid · Zinc Sulfate · Aloe Barbadensis Leaf Juice · Sodium Chloride · Trisodium Ethylenediamine Disuccinate · Alcohol · Dimethyl Lauramine · CI 42090 (Blue 1) · CI 17200 (Red 33)

Fresh Pear

Soothing White Tea

Sensitive Aloe

Citrus Sunburst

Power Berries

Aqua (Water, Eau) · Glycerin · Cetrimonium Chloride · Lauramine Oxide · Cocamidopropyl Betaine · Sodium Benzoate ·
Parfum (Fragrance) · Citric Acid · Zinc Sulfate · Aloe Barbadensis Leaf Juice · Sodium Chloride · Trisodium Ethylenediamine Disuccinate · Alcohol · Tocopheryl Acetate · Dimethyl Lauramine · Vaccinium Macrocarpon (Cranberry) Fruit Juice · Punica Granatum Fruit Juice · Rubus Idaeus (Raspberry) Juice · CI 15985 (Yellow 6) · CI 17200 (Red 33) · CI 16035 (Red 40)

Spring Water

Sensitive & Fragrance Free

Aqua (Water, Eau) · Glycerin · Cetrimonium Chloride · Lauramine Oxide · Cocamidopropyl Betaine · Sodium Benzoate ·
Citric Acid · Zinc Sulfate · Aloe Barbadensis Leaf Juice · Sodium Chloride · Trisodium Ethylenediamine Disuccinate · Alcohol · Dimethyl Lauramine

Questions

call 1-800-258-DIAL(3425)

Legal Entity

www.dialsoap.com

henkel Bean Logo

R,TM,c2024 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

Foaming Hand Wash

Front and the back of the pack

30 Fresh Pear 30 Spring water 52 Spring Water 10 Spring Water 7.5 Spring Water 7.5 Sensitive aloe 10 Sensitive Aloe 10 Power Berries 7.5 Power Berries 10 Citrus Sunburst 7.5 Citrus sunburst 7.5 Fresh Lavender 7.5 Fr Free 52 Fresh Pear 10 Fresh Pear 7.5 Fresh Pear 10 Coconut Water 7.5 Coconut Water 7.5 White Tea 10 White Tea 30 White Tea

DIAL FOAMING ANTIBACTERIAL DEFENSE SOOTHING WHITE TEA
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-186
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0099 g in 100 mL
WATER (UNII: 059QF0KO0R)	95.627 g in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.512 g in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	0.999 g in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.597 g in 100 mL
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)	0.391 g in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.2 g in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.11 g in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB)	0.1 g in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.072 g in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g in 100 mL
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)	0.000009 g in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.000008 g in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-186-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
2	NDC:54340-186-02	296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
3	NDC:54340-186-03	887 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2023
4	NDC:54340-186-04	6 in 1 CARTON	05/01/2023
4		221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
5	NDC:54340-186-05	8 in 1 CARTON	05/01/2023
5		296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2023

DIAL FOAMING ANTIBACTERIAL SENSITIVE ALOE
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-193
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0099 g in 100 mL
WATER (UNII: 059QF0KO0R)	95.59 g in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.512 g in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	0.999 g in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.597 g in 100 mL
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)	0.391 g in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.2 g in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.11 g in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB)	0.1 g in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.072 g in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-193-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
2	NDC:54340-193-02	296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
3	NDC:54340-193-03	6 in 1 CARTON	05/01/2023
3		221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4	NDC:54340-193-04	8 in 1 CARTON	05/01/2023
4		296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2023

DIAL FOAMING ANTIBACTERIAL DEFENSE CITRUS SUNBURST
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-188
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)	95.553 g in 100 mL
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0099 g in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.51 g in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	0.999 g in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.597 g in 100 mL
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)	0.391 g in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.2 g in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.11 g in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB)	0.1 g in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.072 g in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g in 100 mL
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)	0.00022 g in 100 mL
FD&C RED NO. 4 (UNII: X3W0AM1JLX)	0.00014 g in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-188-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
2	NDC:54340-188-02	296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
3	NDC:54340-188-03	6 in 1 CARTON	05/01/2023
3		221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4	NDC:54340-188-05	8 in 1 CARTON	05/01/2023
4		296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2023

DIAL FOAMING ANTIBACTERIAL DEFENSE FRESH LAVENDER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-189
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)	95.5 g in 100 mL
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0099 g in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.51 g in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	0.999 g in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.597 g in 100 mL
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)	0.391 g in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.2 g in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.11 g in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB)	0.1 g in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.072 g in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g in 100 mL
D&C VIOLET NO. 2 (UNII: 350KA7O6HK)	0.000175 g in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-189-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
2	NDC:54340-189-02	6 in 1 CARTON	05/01/2023
2		221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2023

DIAL FOAMING ANTIBACTERIAL DEFENSE FRESH PEAR
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-185
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.597 g in 100 mL
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)	0.391 g in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.2 g in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.11 g in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB)	0.1 g in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.072 g in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g in 100 mL
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)	0.000035 g in 100 mL
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)	0.000027 g in 100 mL
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0099 g in 100 mL
WATER (UNII: 059QF0KO0R)	95.587 g in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.515 g in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	0.999 g in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-185-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
2	NDC:54340-185-02	296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
3	NDC:54340-185-03	887 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2023
4	NDC:54340-185-04	1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2023
5	NDC:54340-185-05	6 in 1 CARTON	05/01/2023
5		221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
6	NDC:54340-185-06	3 in 1 CARTON	05/01/2023
6		1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
7	NDC:54340-185-07	8 in 1 CARTON	05/01/2023
7		296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2023

DIAL FOAMING ANTIBACTERIAL DEFENSE COCONUT WATER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-184
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0099 g in 100 mL
WATER (UNII: 059QF0KO0R)	95.62 g in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.512 g in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	0.999 g in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.597 g in 100 mL
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)	0.391 g in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.2 g in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.11 g in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB)	0.1 g in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.072 g in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g in 100 mL
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)	0.000023 g in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.00001 g in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-184-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
2	NDC:54340-184-02	296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
3	NDC:54340-184-03	8 in 1 CARTON	05/01/2023
3		296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4	NDC:54340-184-04	6 in 1 CARTON	05/01/2023
4		221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2023

DIAL FOAMING ANTIBACTERIAL DEFENSE POWER BERRIES
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-191
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
RUBUS IDAEUS WHOLE (UNII: 7GOM628K2Z)	0.0015 g in 100 mL
VACCINIUM MACROCARPON WHOLE (UNII: D11KO7O2DX)	0.0015 g in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	0.999 g in 100 mL
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0099 g in 100 mL
WATER (UNII: 059QF0KO0R)	95.5 g in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.53 g in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.597 g in 100 mL
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)	0.391 g in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.2 g in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.11 g in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB)	0.1 g in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.072 g in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g in 100 mL
FD&C RED NO. 40 (UNII: WZB9127XOA)	0.000014 g in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.000008 g in 100 mL
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)	0.000064 g in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-191-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
2	NDC:54340-191-02	296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
3	NDC:54340-191-04	8 in 1 CARTON	05/01/2023
3		296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4	NDC:54340-191-03	6 in 1 CARTON	05/01/2023
4		221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2023

DIAL FOAMING ANTIBACTERIAL SENSITIVE FRAGRANCE FREE
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-194
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0099 g in 100 mL
WATER (UNII: 059QF0KO0R)	95.7 g in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.515 g in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	0.999 g in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.597 g in 100 mL
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)	0.391 g in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.2 g in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.11 g in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB)	0.1 g in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.072 g in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-194-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
2	NDC:54340-194-02	6 in 1 CARTON	05/01/2023
2		221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2023

DIAL FOAMING ANTIBACTERIAL DEFENSE SPRING WATER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-195
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
DIMETHYL LAURAMINE (UNII: 6V2OM30I1Z)	0.0099 g in 100 mL
WATER (UNII: 059QF0KO0R)	95.6 g in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.512 g in 100 mL
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	0.999 g in 100 mL
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)	0.597 g in 100 mL
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)	0.391 g in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.2 g in 100 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.11 g in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB)	0.1 g in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0997 g in 100 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X)	0.072 g in 100 mL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)	0.0185 g in 100 mL
ALCOHOL (UNII: 3K9958V90M)	0.013 g in 100 mL
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)	0.000054 g in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.00003 g in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-195-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
2	NDC:54340-195-02	296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023
3	NDC:54340-195-03	887 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2023
4	NDC:54340-195-04	1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2023
5	NDC:54340-195-05	6 in 1 CARTON	05/01/2023
5		221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
6	NDC:54340-195-06	8 in 1 CARTON	05/01/2023
6		296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
7	NDC:54340-195-07	3 in 1 CARTON	05/01/2023
7		1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2023

Labeler - Henkel Corporation (080887708)