DailyMed - DIAL COMPLETE LIMITED EDITION FHW MIDNIGHT TOAST solution DIAL COMPLETE CG FHW GRAPEFRUIT solution DIAL COMPLETE CG FHW FRAGRANCE FREE solution DIAL COMPLETE CG FHW ALOE solution DIAL COMPLETE FHW COCONUT WATER solution DIAL COMPLETE FHW FRESH LAVENDAR solution DIAL COMPLETE 2IN1 FHW MINT AND SHEA solution DIAL COMPLETE 2IN1 FHW PEARL ESSENCE solution DIAL COMPLETE FRESH PEAR FHW solution DIAL COMPLETE SPRING WATER FHW solution DIAL COMPLETE FHW SOOTHING WHITE TEA solution DIAL COMPLETE FHW POWER BERRIES solution DIAL COMPLETE 2IN1 FHW MANUKA HONEY solution DIAL COMPLETE 2IN1 FHW ROSE OIL solution DIAL COMPLETE FHW CITRUS SUNBURST solution DIAL COMPLETE FHW SILK AND SEABERRY solution DIAL COMPLETE LIMITED EDITION FHW FIRESIDE CRACKLE solution DIAL COMPLETE LIMITED EDITION FHW ICE CRYSTALS solution

NDC Code(s): 54340-149-01, 54340-149-02, 54340-149-03, 54340-149-04, view more
54340-149-05, 54340-150-01, 54340-150-02, 54340-150-03, 54340-150-04, 54340-150-05, 54340-151-01, 54340-151-02, 54340-152-01, 54340-152-02, 54340-152-03, 54340-152-04, 54340-153-01, 54340-153-02, 54340-153-03, 54340-154-01, 54340-154-02, 54340-155-01, 54340-155-02, 54340-156-02, 54340-156-03, 54340-157-01, 54340-158-01, 54340-159-01, 54340-160-01, 54340-161-04, 54340-162-05, 54340-163-06, 54340-163-07, 54340-168-02, 54340-169-03, 54340-170-04
Packager: Henkel Corporation

Category: HUMAN OTC DRUG LABEL
DEA Schedule: None

Drug Label Information

Updated November 27, 2023

If you are a consumer or patient please visit this version.

Download DRUG LABEL INFO: PDF XML
Official Label (Printer Friendly)

View All Sections

Drug Facts
Active Ingredient

Benzalkonium Chloride 0.13%
Purpose

Antibacterial
Uses

For Handwashing to decrease 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 a 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 in to DRY hands.
- Lather vigorously for alteast 15 seconds.
- Rinse and dry thoroughly.
INACTIVE INGREDIENT

Spring Water

Inactive Ingredients: Aqua (Water, Eau) · Glycerin · Lauramine Oxide · Cetrimonium Chloride · Cocamidopropyl Betaine ·
Citric Acid · Sodium Benzoate · Hydroxypropyl Methylcellulose · Parfum (Fragrance) · Zinc Sulfate · Sodium Chloride·
Dimethyl Lauramine · Tetrasodium EDTA · Alcohol· Dimethyl Myristamine · Cl 42090 (Blue 1) · Cl 17200 (Red 33)

Citrus
Inactive Ingredients: Aqua (Water, Eau) · Glycerin · Lauramine Oxide · Cetrimonium Chloride · Cocamidopropyl Betaine ·
Citric Acid · Parfum (Fragrance) · Sodium Benzoate · Hydroxypropyl Methylcellulose · Zinc Sulfate· Sodium Chloride ·
Dimethyl Lauramine · Tetrasodium EDTA · Alcohol· Dimethyl Myristamine · Cl 14700 (Red 4) · Cl 15985 (Yellow 6)

Coconut Water
Inactive Ingredients: Aqua (Water, Eau) · Glycerin · Lauramine Oxide · Cetrimonium Chloride · Cocamidopropyl Betaine ·
Citric Acid · Sodium Benzoate · Parfum (Fragrance) · Hydroxypropyl Methylcellulose · Zinc Sulfate · Sodium Chloride ·
Dimethyl Lauramine · Tetrasodium EDTA · Alcohol· Dimethyl Myristamine · Cl 42090 (Blue 1) · Cl 17200 (Red 33)

Lavendar Jasmine
Inactive Ingredients: Aqua (Water, Eau) · Glycerin · Lauramine Oxide · Cetrimonium Chloride · Cocamidopropyl Betalne ·
Citric Acid · Parfum (Fragrance) · Sodium Benzoate · Hydroxypropyl Methylcellulose · Zinc Sulfate· Sodium Chloride ·
Dimethyl Lauramine · Tetrasodium EDTA · Alcohol · Dimethyl Myristamlne · Cl 60730 (Ext. Violet 2)

Fresh Pear
Inactive Ingredients: Aqua (Water, Eau) · Glycerin · Lauramine Oxide · Cetrimonium Chloride · Cocamidopropyl Betaine •
Citric Acid • Sodium Benzoate · Hydroxypropyl Methylcellulose · Parfum (Fragrance)· Zinc Sulfate· Sodium Chloride•
Dimethyl Lauramine · Tetrasodium EDTA · Alcohol · Dimethyl Myristamine , Cl 47005 (Yellow 1 0) · Cl 42053 (Green 3)

Power Berries
nactive Ingredients: Aqua (Waler, Eau) · Glycerin · Lauramine Oxide · Cetrimonium Chloride · Cocamldopropyl Betaine ·
Citric Acid · Sodium Benzoate · Parfum (Fragrance) · Hydroxypropyl Methylcellulose · Zinc Sulfate · Sodium Chloride ·
Dimethyl Lauramine · Tetrasodium EDTA · Alcohol · Dimethyl Myristamine · Tocopheryl Acetate ·
Vaccinium Macrocarpon (Cranberry) Fruit Juice · Punica Granatum Fruit Juice · Rubus ldaeus (Raspberry) Juice·
Cl 17200 (Red 33) · Cl 15510 (Orange 4)

Silk and Seaberry
Inactive Ingredients: Aqua (Waler, Eau) · Glycerin · Lauramine Oxide · Cetrimonium Chloride · Cocamidopropyl Betaine ·
Citric Acid · Sodium Benzoate · Parfum (Fragrance) · Hydroxypropyl Methylcellulose · Zinc Sulfate· Sodium Chloride·
Dimethyl Lauramine · Tetrasodium EDTA, Alcohol· Dimethyl Myristamine · Cl 15985 (Yellow 6) · Cl 14700 (Red 4)

White Tea
Inactive Ingredients: Aqua (Water, Eau) · Glycerin · Lauramine Oxide · Cetrimonium Chloride · Cocamidopropyl Betaine ·
Citric Acid · Sodium Benzoate · Hydroxypropyl Methylcellulose · Parfum (Fragrance)· Zinc Sulfate· Sodium Chloride·
Dimethyl Lauramine · Tetrasodium EDTA · Alcohol· Dimethyl Myristamine · Cl 42090 (Blue 1) · Cl 17200 (Red 33)

2in1 Manuka Honey
Inactive Ingredients: Aqua (Water, Eau) · Lauramidopropylamine Oxide · Glycerin · Cetrimonium Chloride · Lauramine Oxide ·
Citric Acid · Cocamidopropyl Betaine · Parfum (Fragrance) · Trideceth-9 · Sodium Benzoate · Myristamidopropylamine Oxide ·
Hydroxypropyl Methylcellulose · PEG-5 lsononanoate · Zinc Sulfate· Sodium Chloride· Dimethyl Lauramine · Tetrasodium EDTA
·Alcohol· Dimethyl Myristamine · Mel (Honey)· Cl 19140 (Yellow 5) · Cl 14700 (Red 4)

2in1 Mint Shea
Inactive Ingredients: Aqua (Water, Eau) · Lauramidopropylamine Oxide · Cetrimonium Chloride · Glycerin · Lauramine Oxide ·
Citric Acid · Cocamidopropyl Betaine · Trideceth-9 · Sodium Benzoate · Parfum (Fragrance) · Myristamidopropylamine Oxide ·
Hydroxypropyl Methylcellulose · PEG-5 lsononanoate · Zinc Sulfate· Sodium Chloride· Dimethyl Lauramine · Tetrasodium EDTA
·Alcohol· Dimethyl Myristamine · Cl 42090 (Blue 1) · Cl 47005 (Yellow 10)

2in1 Pearl Essence
Inactive Ingredients: Aqua (Water, Eau) · Lauramidopropylamine Oxide · Glycerin · Cetrimonium Chloride · Lauramine Oxide ·
Citric Acid · Cocamidopropyl Betaine · Trideceth-9 · Sodium Benzoate · Parfum (Fragrance) · Myristamidopropylamine Oxide ·
Hydroxypropyl Methylcellulose· PEG-5 lsononanoate · Zinc Sulfate· Sodium Chloride· Dimethyl Lauramine · Tetrasodium EDTA ·
Alcohol· Dimethyl Myristamine · Maris Sal (Sea Salt)· Hydrolyzed Pearl· Cl 42090 (Blue 1) · Cl 17200 (Red 33)

2in1 Rose Oil
Inactive Ingredients: Aqua (Water, Eau) · Lauramidopropylamine Oxide · Glycerin · Cetrimonium Chloride · Lauramine Oxide ·
Citric Acid · Cocamidopropyl Betaine · Trideceth-9 · Sodium Benzoate · Parfum (Fragrance) · Myristamidopropylamine Oxide ·
Hydroxypropyl Methylcellulose· PEG-5 lsononanoate · Zinc Sulfate· Sodium Chloride· Dimethyl Lauramine · Tetrasodium EDTA ·
Alcohol· Dimethyl Myristamine · Rosa Damascena Flower Oil· Cl 15985 (Yellow 6) · Cl 17200 (Red 33) · Cl 16035 (Red 40)

Clean Gentle FHW Aloe
Inactive Ingredients: Aqua (Water, Eau)· Glycerin · Lauramine Oxide · Cetrimonium Chloride ·
Cocamidopropyl Betaine · Citric Acid, Sodium Benzoate · Parfum (Fragrance) · Zinc Sulfate· Sodium Chloride· Dimethyl Lauramine · Tetrasodium EDTA ·Alcohol· Dimethyl Myristamine

Clean Gentle Grapefruit

Inactive Ingredients: Aqua (Water, Eau)· Glycerin · Lauramine Oxide · Cetrimonium Chloride ·
Cocamidopropyl Betaine · Citric Acid, Sodium Benzoate · Parfum (Fragrance) · Zinc Sulfate· Sodium Chloride· Dimethyl Lauramine · Tetrasodium EDTA ·Alcohol· Dimethyl Myristamine

Clean Gentle FHW Fragrance Free

Inactive Ingredients: Aqua (Water, Eau)· Glycerin · Lauramine Oxide · Cetrimonium Chloride ·
Cocamidopropyl Betaine · Citric Acid, Sodium Benzoate · Zinc Sulfate· Sodium Chloride· Dimethyl Lauramine · Tetrasodium EDTA ·Alcohol· Dimethyl Myristamine

Dial Complete Limited Edition FHW Midnight Toast

Aqua (Water, Eau)· Glycerin · Lauramine Oxide · Cetrimonium Chloride ·
Cocamidopropyl Betaine · Citric Acid, Sodium Benzoate · Parfum (Fragrance)· Zinc Sulfate· Sodium Chloride· Dimethyl Lauramine · Tetrasodium EDTA ·Alcohol· Dimethyl Myristamine

Dial Complete Limited Edition FHW Ice Crystals

Aqua (Water, Eau)· Glycerin · Lauramine Oxide · Cetrimonium Chloride ·
Cocamidopropyl Betaine · Citric Acid, Sodium Benzoate · Parfum (Fragrance)· Zinc Sulfate· Sodium Chloride· Dimethyl Lauramine · Tetrasodium EDTA ·Alcohol· Dimethyl Myristamine

Dial Complete Limited Edition FHW Fireside Crackle

Aqua (Water, Eau)· Glycerin · Lauramine Oxide · Cetrimonium Chloride ·
Cocamidopropyl Betaine · Citric Acid, Sodium Benzoate · Parfum (Fragrance)· Zinc Sulfate· Sodium Chloride· Dimethyl Lauramine · Tetrasodium EDTA ·Alcohol· Dimethyl Myristamine
SPL UNCLASSIFIED SECTION

Encountered in household settings

#Antibacterial Hand Soap
Questions

? 1-800-258-DIAL (3425)
Legal entity

®,TM,©2019 Distributed by Henkel
Corporation, Rocky Hill CT 06067
Refill Instruction

Use only in DIAL COMPLETE®
FOAMING HAND WASH
pumps. REFILL ONLY TO
BACK LABEL FILL LINE. Filling
past the line may cause pump
to stick. If overfill
occurs, wipe with
damp towel. Do not
rinse the pump
under water.
INDICATIONS & USAGE

Kills 99.99% bacteria.

For handwashing to decrease bacteria on the skin.
Topical

Foaming Hand wash
Principle display

INGREDIENTS AND APPEARANCE

DIAL COMPLETE LIMITED EDITION FHW MIDNIGHT TOAST
dial complete limited edition fhw midnight toast solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-170
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)	94.23 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54340-170-04	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE CG FHW GRAPEFRUIT
dial complete cg fhw grapefruit solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-162
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)	94.23 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54340-162-05	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE CG FHW FRAGRANCE FREE
dial complete cg fhw fragrance free solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-163
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)	94.23 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-163-06	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC:54340-163-07	325 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE CG FHW ALOE
dial complete cg fhw aloe solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-161
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)	94.23 mL in 100 mL

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54340-161-04	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE FHW COCONUT WATER
dial complete fhw coconut water solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-153
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)	94.23 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-153-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC:54340-153-02	296 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
3	NDC:54340-153-03	444 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE FHW FRESH LAVENDAR
dial complete fhw fresh lavendar solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-151
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)	94.01 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-151-01	296 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC:54340-151-02	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE 2IN1 FHW MINT AND SHEA
dial complete 2in1 fhw mint and shea solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-160
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)	91.24 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54340-160-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE 2IN1 FHW PEARL ESSENCE
dial complete 2in1 fhw pearl essence solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-159
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)	91.15 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54340-159-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE FRESH PEAR FHW
dial complete fresh pear fhw solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-150
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)	94.3 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-150-02	946 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC:54340-150-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
3	NDC:54340-150-03	1180 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
4	NDC:54340-150-04	296 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
5	NDC:54340-150-05	1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE SPRING WATER FHW
dial complete spring water fhw solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-149
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)	94.27 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-149-02	946 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC:54340-149-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
3	NDC:54340-149-03	1180 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
4	NDC:54340-149-04	296 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
5	NDC:54340-149-05	1530 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE FHW SOOTHING WHITE TEA
dial complete fhw soothing white tea solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-152
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)	94.32 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-152-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC:54340-152-02	296 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
3	NDC:54340-152-03	946 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
4	NDC:54340-152-04	444 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE FHW POWER BERRIES
dial complete fhw power berries solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-155
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)	94.19 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-155-02	296 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC:54340-155-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE 2IN1 FHW MANUKA HONEY
dial complete 2in1 fhw manuka honey solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-157
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)	91.05 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54340-157-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE 2IN1 FHW ROSE OIL
dial complete 2in1 fhw rose oil solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-158
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)	91.22 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54340-158-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE FHW CITRUS SUNBURST
dial complete fhw citrus sunburst solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-156
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)	94.03 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-156-02	296 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC:54340-156-03	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE FHW SILK AND SEABERRY
dial complete fhw silk and seaberry solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-154
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)	94.23 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:54340-154-01	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020
2	NDC:54340-154-02	296 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE LIMITED EDITION FHW FIRESIDE CRACKLE
dial complete limited edition fhw fireside crackle solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-168
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)	94.23 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54340-168-02	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

DIAL COMPLETE LIMITED EDITION FHW ICE CRYSTALS
dial complete limited edition fhw ice crystals solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54340-169
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)	94.23 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54340-169-03	221 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2020

Labeler - Henkel Corporation (080887708)

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Published Date (What is this?)	Version	Files
Nov 28, 2023	10 (current)	download
Sep 19, 2022	9	download
Apr 4, 2022	7	download
Mar 16, 2022	6	download
Dec 28, 2021	5	download
Dec 24, 2021	4	download
Dec 22, 2021	3	download
Jul 16, 2020	2	download
May 4, 2020	1	download

	RxCUI	RxNorm NAME	RxTTY
1	1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN
2	1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD
3	1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY
4	1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY
5	1049254	benzalkonium chloride 0.13 % Topical Solution	PSN
6	1049254	benzalkonium chloride 1.3 MG/ML Topical Solution	SCD
7	1049254	benzalkonium chloride 0.13 % Topical Solution	SY

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	NDC
1	54340-149-01
2	54340-149-02
3	54340-149-03
4	54340-149-04
5	54340-149-05
6	54340-150-01
7	54340-150-02
8	54340-150-03
9	54340-150-04
10	54340-150-05
11	54340-151-01
12	54340-151-02
13	54340-152-01
14	54340-152-02
15	54340-152-03
16	54340-152-04
17	54340-153-01
18	54340-153-02
19	54340-153-03
20	54340-154-01
21	54340-154-02
22	54340-155-01
23	54340-155-02
24	54340-156-02
25	54340-156-03
26	54340-157-01
27	54340-158-01
28	54340-159-01
29	54340-160-01
30	54340-161-04
31	54340-162-05
32	54340-163-06
33	54340-163-07
34	54340-168-02
35	54340-169-03
36	54340-170-04

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If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.