Active Ingredient(S)
Benzalkonium chloride 0.13%
Hand Antibacterial Wipes
FDA Label NDC 76991-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hefei Wenqi Industrial & Trade Co., Ltd for the product Hand Antibacterial Wipes (NDC 76991-009). 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(s), purpose, use, do not use, otc - when using, otc - 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
Sanitizer to reduce bacteria and virus on surfaces
Do Not Use
Do not use in or contact the eyes
Discontinue useif irritation and redness develop. if condition persists for more than 72 hours consult a physician.
Otc - When Using
Pull through about one inch. Replace cover Pull out wipes as needed and snap off at a 90° angle. Keep cap closed to prevent evaporation
Wipe hands, fingers, interdigital areas and wrists thoroughly with towelette. Be sure to utilize the entire wipe surface, Allow to dry
lf hands are visibly soiled or contaminated use first wipe to clean hands then discard wipe Sanitize with a second wipe discard after single use.
Otc - Stop Use
/
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
Wet the surface with the product and allow to dry
Children under 6 years old should bebe supervised when using this product
Inactive Ingredients
decyl glucoside
Glycerin
water
Package Label.Principal Display Panel
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