Dial Hand Sanitzer (Gel/Foaming)
Dial Professional Gel Hand Sanitizer
Active Ingredient: Ethyl Alcohol 62.0% v/v Purpose: Antiseptic
Dial Professional Gel Sanitizer Gel
FDA Label NDC 54340-136
5 label sections · Submitted to the FDA by Henkel Corporation · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Henkel Corporation for the product Dial Professional Gel Sanitizer (NDC 54340-136). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding dial hand sanitzer (gel/foaming), warnings, dosage & administration, indications & usage, inactive ingredient, dial gel/foaming hand sanitizer, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
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
* Please review the disclaimer below.
