Label: 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
-
NDC Code(s):
54340-173-01,
54340-173-02,
54340-173-03,
54340-173-04, view more54340-174-01, 54340-174-02, 54340-175-01, 54340-175-02, 54340-176-01, 54340-176-02, 54340-177-01, 54340-177-02, 54340-181-01, 54340-181-02, 54340-182-01, 54340-182-02, 54340-182-03, 54340-182-04, 54340-183-01, 54340-183-02, 54340-183-03, 54340-183-04
- Packager: Henkel Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Uses
- Warnings
- When Using this Product
- Stop use and ask doctor if
- Keep out of reach of children.
- 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 · AlcoholVariant 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
- Legal Entity
- ^Encountered in household settings
- Indications & Usage
- Topical Liquid
- Front and the back of the pack
-
INGREDIENTS AND APPEARANCE
DIAL ANTIBACTERIAL DEFENSE SPRING WATER
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-183 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:54340-183-01 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2023 2 NDC:54340-183-02 1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 05/01/2023 3 NDC:54340-183-03 12 in 1 CARTON 05/01/2023 3 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 4 NDC:54340-183-04 3 in 1 CARTON 05/01/2023 4 1530 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) 05/01/2023 DIAL ANTIBACTERIAL AND SENSITIVE FRAGRANCE FREE
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-174 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:54340-174-01 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2023 2 NDC:54340-174-02 12 in 1 CARTON 05/01/2023 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) 05/01/2023 DIAL ANTIBACTERIAL DEFENSE WHITE TEA
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-176 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 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-176-01 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2023 2 NDC:54340-176-02 12 in 1 CARTON 05/01/2023 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) 05/01/2023 DIAL ANTIBACTERIAL DEFENSE POMEGRANATE AND TANGERINE
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-177 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 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-177-01 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2023 2 NDC:54340-177-02 12 in 1 CARTON 05/01/2023 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) 05/01/2023 DIAL ANTIBACTERIAL AND SENSITIVE ALOE
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-182 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) 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-182-01 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2023 2 NDC:54340-182-02 1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 05/01/2023 3 NDC:54340-182-03 12 in 1 CARTON 05/01/2023 3 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 4 NDC:54340-182-04 3 in 1 CARTON 05/01/2023 4 1530 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) 05/01/2023 DIAL ANTIBACTERIAL DEFENSE LAVENDER AND JASMINE
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-175 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) 89.5 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-175-01 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2023 2 NDC:54340-175-02 12 in 1 CARTON 05/01/2023 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) 05/01/2023 DIAL ANTIBACTERIAL DEFENSE GOLD
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-173 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:54340-173-01 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2023 2 NDC:54340-173-02 1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 05/01/2023 3 NDC:54340-173-03 12 in 1 CARTON 05/01/2023 3 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 4 NDC:54340-173-04 3 in 1 CARTON 05/01/2023 4 1530 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) 05/01/2023 DIAL ANTIBACTERIAL DEFENSE LEMON AND SAGE
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-181 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) 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-181-01 325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2023 2 NDC:54340-181-02 12 in 1 CARTON 05/01/2023 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) 05/01/2023 Labeler - Henkel Corporation (080887708)
