Active Ingredient
Ethyl Alcohol 70%
Wet Wipes
FDA Label NDC 69821-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Qimei Commodity Co.,ltd. for the product Wet Wipes (NDC 69821-003). 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, uses, warnings, keep out of reach of children, directions, inactive ingredient, 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
Uses
●For hand sanitizing to decrease bacteria on the skin
●Recommended for repeated use
Warnings
. FOR EXTERNAL USE ONLY
. FLAMMABL E, KEEP AWAY FROM FIRE OR FL AME
●When using this product avoid contact with eyes. In case of eye contact,
flush eyes with water and seek medical help.
●If swallowed drink large amounts of water and seek medical attention.
●Avoid contact with face and broken skin. If contact occurs, flush with water.
●Stop use and ask a doctor if rritation or redness develops
Note Do not store above00°F. Non-stainingMay discolor some fabrics.
Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
●Take wipe and rub thoroughly over all surfaces of both hands
●Allow to dry without wiping
●Dispose of wipe in trash after use. Do not flush.
Inactive Ingredient
Purfied Water, Anionic Surfactant,
Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice.
* Please review the disclaimer below.
