Active Ingredient
Ethyl Alcohol 70% v/v.
Kellys Delight Hand Sanitizer
FDA Label NDC 79175-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Waco Bottling Llc for the product Kellys Delight Hand Sanitizer (NDC 79175-005). 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, purpose, use, warnings, directions, other information, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease.
For use when soap and water are not available.
Warnings
For external use only.
Flammable. Keep away from heat or flame.
Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
•Wet hands.
•Briskly rub hands together until dry.
•Supervise children in the use of this product.
Other Information
•Store at 20-25C(68-77F)
•Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
Water, Frangrance (Parfum), Glycerin, lsopropyl Myristate, PEG-6 & AMP Acrylates I Vinyl lsodecanoate Crosspolymer, Tocopheryl Acetate.
* Please review the disclaimer below.
