DIAL PROFESSIONAL ORIGINAL GOLD ANTIBACTERIAL- dial professional original gold antibacterial hand soap liquid

Dial Professional Original Gold Antibacterial by

Drug Labeling and Warnings

Dial Professional Original Gold Antibacterial by is a Otc medication manufactured, distributed, or labeled by Henkel Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Dial® Professional Original Gold Antibacterial Liquid Hand Soap

Aqua (Water, Eau)
Lauramidopropylamine Oxide
Glycerin
Cetrimonium Chloride
Lauramine Oxide
Sodium Chloride
PEG-120 Methyl Glucose Dioleate
Citric Acid
Sodium Benzoate
Myristamidopropylamine Oxide
Zinc Sulfate
Parfum (Fragrance)
Dimethyl Lauramine
Tetrasodium EDTA
Hydrogen Peroxide
Alcohol
Dimethyl Myristamine
CI 19140 (Yellow 5)

CI 14700 (Red 4)

Warnings

Warnings For external use only

When using this productAvoid contact with eyes

Stop use and ask a doctor ifIrritation or redness develops OR Stop use and ask a doctor ifirritation or redness develops
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

Uses

For hand washing to decrease bacteria on the skin

Dial Professional Original Gold Antibacterial Liquid Hand Soap

Benzalkonium Chloride

KEEP OUT OF REACH OF CHILDREN

PURPOSE

Dial® Professional Original Gold Antibacterial Liquid Hand Soap

INGREDIENTS AND APPEARANCE

DIAL PROFESSIONAL ORIGINAL GOLD ANTIBACTERIAL 
dial professional original gold antibacterial hand soap liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-135
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
WATER (UNII: 059QF0KO0R)	90.54 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-135-04	144 in 1 CARTON	02/01/2021
1	NDC: 54340-135-03	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 54340-135-02	12 in 1 CARTON	01/01/2017
2	NDC: 54340-135-01	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 54340-135-06	12 in 1 CARTON	01/01/2017
3	NDC: 54340-135-05	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4	NDC: 54340-135-08	8 in 1 CARTON	01/01/2017
4	NDC: 54340-135-07	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
5	NDC: 54340-135-10	4 in 1 CARTON	01/01/2017
5	NDC: 54340-135-09	3785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
6	NDC: 54340-135-12	6 in 1 CARTON	01/01/2017
6	NDC: 54340-135-11	443 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)	01/01/2017

Labeler - Henkel Corporation (080887708)