DIAL PROFESSIONAL GEL SANITIZER- dial professional gel hand sanitizer gel

Dial Professional Gel Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Dial Hand Sanitzer (Gel/Foaming)

Dial Professional Gel Hand Sanitizer

Active Ingredient: Ethyl Alcohol 62.0% v/v Purpose: Antiseptic

Warnings

Warnings For external use only
Flammable. Keep away from fire or flame.

When using this productAvoid contact with face, eyes, and broken skin. If eye contact occurs, flush thoroughly with water and seek medical advice.ORWhen using this productavoid contact with face, eyes, and broken skin.If eye contact occurs, flush thoroughly with water and seek medical advice.
Stop use and ask a doctor ifIrritation or redness developsORStop 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

Use(s)Hand sanitizer to help reduce bacteria thatpotentially may cause disease

INDICATIONS & USAGE

Use(s)Hand sanitizer to help reduce bacteria that potentially may cause disease

INACTIVE INGREDIENT

Inactive ingredients Aqua (Water, Eau) · Propylene Glycol ·

Glycerin . Carbomer . Aminomethyl Propanol . Isopropyl Myristate .
T-Butyl Alcohol

KEEP OUT OF REACH OF CHILDREN

PURPOSE

Dial Gel/Foaming Hand Sanitizer

INGREDIENTS AND APPEARANCE

DIAL PROFESSIONAL GEL SANITIZER 
dial professional gel hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-136
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60.14 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	38.19 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-136-02	3 in 1 CARTON	06/21/2022	01/01/2024
1	NDC: 54340-136-01	1200 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
2	NDC: 54340-136-04	12 in 1 CARTON	06/21/2022	01/01/2024
2	NDC: 54340-136-03	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 54340-136-06	6 in 1 CARTON	06/21/2022	01/01/2024
3	NDC: 54340-136-05	443 mL in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 54340-136-08	3 in 1 CARTON	06/21/2022	01/01/2024
4	NDC: 54340-136-07	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
5	NDC: 54340-136-10	144 in 1 CARTON	06/21/2022	01/01/2024
5	NDC: 54340-136-09	59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
6	NDC: 54340-136-11	12 in 1 CARTON	01/01/2024
6		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)	06/21/2022

Labeler - Henkel Corporation (080887708)