DIAL ANTIBACTERIAL DEFENSE SPRING WATER- benzalkonium chloride solution 
DIAL ANTIBACTERIAL AND SENSITIVE FRAGRANCE FREE- benzalkonium chloride solution 
DIAL ANTIBACTERIAL DEFENSE WHITE TEA- benzalkonium chloride solution 
DIAL ANTIBACTERIAL DEFENSE POMEGRANATE AND TANGERINE- benzalkonium chloride solution 
DIAL ANTIBACTERIAL AND SENSITIVE ALOE- benzalkonium chloride solution 
DIAL ANTIBACTERIAL DEFENSE LAVENDER AND JASMINE- benzalkonium chloride solution 
DIAL ANTIBACTERIAL DEFENSE GOLD- benzalkonium chloride solution 
DIAL ANTIBACTERIAL DEFENSE LEMON AND SAGE- benzalkonium chloride solution 
Henkel Corporation

----------

Dial Antibacterial Defense Hand Soap
Dial Antibacterial Hand Soap
Dial Antibacterial & Sensitive Hand Soap
Dial Antibacterial Defense Hand Soap Gold
Dial Antibacterial Defense Hand Soap Lavender & Jasmine
Dial Antibacterial Defense Hand Soap White Tea
Dial Antibacterial Defense Hand Soap Lemon & Sage
Dial Antibacterial & Sensitive Hand Soap Aloe
Dial Antibacterial Defense Hand Soap Spring Water
Dial Antibacterial & Sensitive Hand Soap Fragrance Free

Drug Facts

Drug Facts Table

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

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 Lav & Jasmine:

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 17200 (Red 33). CI 42090 (Blue 1)

Variant White Tea:

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 · Camellia Sinensis Leaf Extract · CI 42090

(Blue 1) · CI 17200 (Red 33)

Variant Pom & Tangerine:

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 15985 (Yellow 6) · CI 17200 (Red 33) · CI16035 (Red 40)

Variant AB & Sensitive Aloe:

Inactive ingredients: Aqua (Water, Eau) · Lauramidopropylamine Oxide · Sodium Chloride · 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

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 Lemon & Sage:

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 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

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

AB White Tea 11 ozAB Defense AloeDial Frag FreeLemon and Sage 11 ozLav and Jas 11 ozSensitive Aloe 11 ozAB Gold 11 ozAb Gold REfillSW refillAB Sensitive Aloe Refill

DIAL ANTIBACTERIAL DEFENSE SPRING WATER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-183
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-183-01325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2023
2NDC:54340-183-021530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2023
3NDC:54340-183-0312 in 1 CARTON05/01/2023
3325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4NDC:54340-183-043 in 1 CARTON05/01/2023
41530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/01/2023
DIAL ANTIBACTERIAL AND SENSITIVE FRAGRANCE FREE 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-174
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-174-01325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2023
2NDC:54340-174-0212 in 1 CARTON05/01/2023
2325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/01/2023
DIAL ANTIBACTERIAL DEFENSE WHITE TEA 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-176
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ) 0.01 g  in 100 mL
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 BLUE NO. 1 (UNII: H3R47K3TBD) 0.000009 g  in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L) 0.000008 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-176-01325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2023
2NDC:54340-176-0212 in 1 CARTON05/01/2023
2325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/01/2023
DIAL ANTIBACTERIAL DEFENSE POMEGRANATE AND TANGERINE 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-177
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ) 0.01 g  in 100 mL
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 g  in 100 mL
FD&C YELLOW NO. 6 (UNII: H77VEI93A8) 0.000127 g  in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L) 0.000109 g  in 100 mL
FD&C RED NO. 40 (UNII: WZB9127XOA) 0.000027 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-177-01325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2023
2NDC:54340-177-0212 in 1 CARTON05/01/2023
2325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/01/2023
DIAL ANTIBACTERIAL AND SENSITIVE ALOE 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-182
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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) 90.43 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) 1.55 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-182-01325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2023
2NDC:54340-182-021530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2023
3NDC:54340-182-0312 in 1 CARTON05/01/2023
3325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4NDC:54340-182-043 in 1 CARTON05/01/2023
41530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/01/2023
DIAL ANTIBACTERIAL DEFENSE LAVENDER AND JASMINE 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-175
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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) 89.5 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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD) 0.000055 g  in 100 mL
D&C RED NO. 33 (UNII: 9DBA0SBB0L) 0.000099 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-175-01325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2023
2NDC:54340-175-0212 in 1 CARTON05/01/2023
2325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/01/2023
DIAL ANTIBACTERIAL DEFENSE GOLD 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-173
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-173-01325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2023
2NDC:54340-173-021530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2023
3NDC:54340-173-0312 in 1 CARTON05/01/2023
3325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4NDC:54340-173-043 in 1 CARTON05/01/2023
41530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/01/2023
DIAL ANTIBACTERIAL DEFENSE LEMON AND SAGE 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-181
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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) 90 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) 1.8 g  in 100 mL
FD&C YELLOW NO. 5 (UNII: I753WB2F1M) 0.000351 g  in 100 mL
FD&C RED NO. 4 (UNII: X3W0AM1JLX) 0.000003 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-181-01325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2023
2NDC:54340-181-0212 in 1 CARTON05/01/2023
2325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/01/2023
Labeler - Henkel Corporation (080887708)

Revised: 12/2023
Document Id: 0c53cf6c-7f69-98aa-e063-6394a90a149d
Set id: 0a34b1b4-ad14-43b7-e063-6394a90a570f
Version: 2
Effective Time: 20231212
 
Henkel Corporation