DIAL ANTIBACTERIAL DEFENSE SANDALWOOD VANILLA- benzalkonium chloride solution DIAL ANTIBACTERIAL DEFENSE ORCHID ROSE BLISS SCENT- benzalkonium chloride solution DIAL ANTIBACTERIAL DEFENSE EUCALYPTUS MINT- benzalkonium chloride solution DIAL ANTIBACTERIAL DEFENSE PEACH CITRUS PUNCH SCENT- benzalkonium chloride solution

Dial Antibacterial Defense Peach Citrus Punch Scent by

Drug Labeling and Warnings

Dial Antibacterial Defense Peach Citrus Punch Scent 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 Orchid Rose Bliss (Limited Edition):

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) · Aloe Barbadensis Leaf Juice · Zinc Sulfate · Trisodium Ethylenediamine Disuccinate · Dimethyl Lauramine · Alcohol · CI 17200 (Red 33) · CI 19140 (Yellow 5)

Variant Peach Citrus Punch (Limited Edition):

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) · Aloe Barbadensis Leaf Juice · Zinc Sulfate · Trisodium Ethylenediamine Disuccinate · Dimethyl Lauramine · Alcohol · CI 14700 (Red 4) · CI 17200 (Red 33)

Variant Sandalwood and Vanilla:

Aqua (Water, Eau) · Lauramidopropylamine Oxide · Glycerin · Cetrimonium Chloride · Sodium 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 19140 (Yellow 5) · CI 17200 (Red 33) · CI 42090 (Blue 1)

Variant Eucalyptus & Mint:

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) · Aloe Barbadensis Leaf Juice · Zinc Sulfate · Trisodium Ethylenediamine Disuccinate · Dimethyl Lauramine · Alcohol · CI 15985 (Yellow 6) · CI 42090 (Blue 1) · CI 17200 (Red 33)

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

Liquid Hand Soap

Front and the back of the pack

INGREDIENTS AND APPEARANCE

DIAL ANTIBACTERIAL DEFENSE SANDALWOOD VANILLA 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-133
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)
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)
WATER (UNII: 059QF0KO0R)
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)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)	0.000036 g  in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.000099 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-133-02	325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/07/2024
2	NDC: 54340-133-01	12 in 1 CARTON	01/07/2024
2		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)	01/07/2024

DIAL ANTIBACTERIAL DEFENSE ORCHID ROSE BLISS SCENT 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-131
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)
WATER (UNII: 059QF0KO0R)
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)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)	0.000036 g  in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.000099 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-131-02	325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2025
2	NDC: 54340-131-01	12 in 1 CARTON	06/01/2025
2		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)	06/01/2025

DIAL ANTIBACTERIAL DEFENSE EUCALYPTUS MINT 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-134
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)
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)
WATER (UNII: 059QF0KO0R)
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)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)	0.000337 g  in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.000099 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-134-02	325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/07/2024
2	NDC: 54340-134-01	12 in 1 CARTON	01/07/2024
2		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)	01/07/2024

DIAL ANTIBACTERIAL DEFENSE PEACH CITRUS PUNCH SCENT 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-132
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)
WATER (UNII: 059QF0KO0R)
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)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)	0.000036 g  in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L)	0.000099 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-132-02	325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2025
2	NDC: 54340-132-01	12 in 1 CARTON	06/01/2025
2		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)	06/01/2025

Labeler - Henkel Corporation (080887708)