Label: DIAL ANTIBACTERIAL GEL HAND SANITIZER gel
- NDC Code(s): 54340-172-16
- 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)
-
Dial Hand Sanitzer (Gel/Foaming)
Dial Professional Gel Hand Sanitizer
Active Ingredient: Ethyl Alcohol 62.0% v/v Purpose: Antiseptic
Inactive Ingredients: Aqua (Water, Eau) · Propylene Glycol · Glycerin · Carbomer · Aminomethyl Propanol · Isopropyl Myristate · T-Butyl Alcohol
Dial Professional Foaming Hand Sanitizer
Active Ingredient: Ethyl Alcohol 65% v/v Purpose: Antiseptic
Inactive Ingredients: Aqua (Water, Eau) · PEG-10 Dimethicone · Glycerin · Cocamidopropyl PG-Dimonium Chloride · Isopropyl Myristate · PEG-12 Allyl Ether · T-Butyl Alcohol · Diazolidinyl Urea · Methylparaben
-
Warnings
Warnings For external use only
Flammable. Keep away from fire or flame.When using this product•Avoid 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 if•Irritation 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
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- Dial Gel/Foaming Hand Sanitizer
-
INGREDIENTS AND APPEARANCE
DIAL ANTIBACTERIAL GEL HAND SANITIZER
dial antibacterial gel hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-172 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.62 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 0.33 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-172-16 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/12/2023 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)
