Active Ingredient
Ethyl Alcohol 70%
Hand Sanitizer Wipes
FDA Label NDC 69821-006
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 Hand Sanitizer Wipes (NDC 69821-006). 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 Handwash
Uses
■ For hand washing to dec rease bacteria on the
skin. Recommended for repeated use.
Warnings
For external use only
Flammable, Keep away from fire or flame
When using this product avoid contact with eyes.
In case of eye contact, rins e with water to remove.
Stop use and ask a doctor if irritation and
redness develop
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
■Wet hands thoroughly wi th product and allow to
dry without wiping.
Inactive Ingredient
Aloe Barbadensis Leaf Juice, Carbormer,Diazolidinyl Urea, Glycerin,Methylparaben,
Polysorbate 20, Propylene Glycol, Propylparaben,Tocopheryl Acetate, Trietha nolamine, Water
* Please review the disclaimer below.
