Active Ingredient
Ethyl Alcohol 75%
Hand Alcohol Wipes
FDA Label NDC 77720-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Skaffles Group Limited Liability Company for the product Hand Alcohol Wipes (NDC 77720-015). 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, warning, otc - keep out of reach of children, directions, 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
For hand washing to decrease bacteria on the skin.
Recommended for repeated use.
Warning
For external use only. Do not use
. If you are allergic to any of the ingredients.. ln the eyes. If contact occurs, rinse
thoroughly with water.
Discontinue use if irritation and redness develop. If condition persists for more than72 hours consult a doctor.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions● Adults and children 2 yrs and over,
apply to hands and allow skin to dry without wiping.
●Children under 2, ask doctor before use.
Inactive Ingredients
Glycerin,Water.
Package Label.Principal Display Panel
1 (2a81527a B666 4843 A4cc B0132b3394c1)
* Please review the disclaimer below.
