Active Ingredient(S)
Ethyl Alcohol 65% v/v. Purpose: Antiseptic
Dial Professional Foaming Hand Sanitizer
FDA Label NDC 50663-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zotos International Inc for the product Dial Professional Foaming Hand Sanitizer (NDC 50663-004). 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 active ingredient(s), purpose, use, warnings, otc - when using, directions, inactive ingredients, questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease.
Warnings
For external use only. Flammable. Keep away from fire or flame
Otc - When Using
When using this product avoid 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 develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Put foam into DRY hands, wet hands thoroughly and rub into skin until dry.
- Children under 6 years of age should be supervised by an adult when using this product.
Inactive Ingredients
Aqua (Water, Eau)· PEG-10 Dimethicone · Glycerin · Cocamidopropyl PG-Dimonium Chloride· lsopropyl Myristate ·
PEG-12 Allyl Ether· T-Butyl Alcohol · Diazolidinyl Urea · Methylparaben
Questions
1-877-777-3277
Legal Entity
®,TM,©2018 Distributed by
Henkel Corporation,
Rocky Hill, CT 06067
www.dialprofessional.com
Package Label - Principal Display Panel
450 mL NDC: 50663-004-01
* Please review the disclaimer below.
