Active Ingredient
Ethyl Alcohol 80%
Fresh Nap Plus Hand Sanitizer Swab
FDA Label NDC 0924-0255
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Acme United Corporation for the product Fresh Nap Plus Hand Sanitizer (NDC 0924-0255). 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, do not use, stop use, otc - keep out of reach of children, directions, 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 on the skin
Warnings
For external use only
Flammable. Keep away from fire or flame
Do Not Use
▪in eyes. If contact occurs, flush with water.
▪on open wounds
▪on children less than 2 months of age
Stop Use
if irritation occurs
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Unfold towelette, wipe hands thoroughly, and discard.
Inactive Ingredients
glycerin, hydrogen peroxide, purified water
Package Label.Principal Display Panel
Packette Label (840277 Reva Fda)
* Please review the disclaimer below.
