Active Ingredient
Ethanol 75%
Wet Wipe
FDA Label NDC 75513-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Onecare Products Llc for the product Wet Wipe (NDC 75513-001). 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 sanitizing to decrease bacteria on the skin.
Apply topically to the skin to help prevent cross contamination.
Recommended for repeated use.
Dries in seconds.
If swallowed, get medical help or contact a Poison Control Center
immediately.
Warning
●Flammable, Keep away from fire or flame. For external use only.
Do not use in or contact the eyes.
●Discontinue use if rritation and redness develop. If condition persist
for more than 72 hours, consult a physician.
Otc - Keep Out Of Reach Of Children
●. Keep out of reach of children unless under adult supervision.
Directions
●Open lid, gently pull back resealable label, remove and use
wipe as required.
●Reseal back after use to avoid evaporation of alcohol.
Inactive Ingredients
Aqua
* Please review the disclaimer below.
