Active Ingredient(S)
Benalkonium Chloride: 0.10%
Vivo Antibacterial Hand Wipes
FDA Label NDC 75177-059
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Herstyler, Inc. for the product Vivo Antibacterial Hand Wipes (NDC 75177-059). 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, warnings, 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
For hand sanitizing to decrease bacteria on the skin
Discard after single use
Warnings
For external use only.
Otc - When Using
When using this product, avoid contacting with eyes. In case of contact with eyes, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops and persists
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, contact a doctor or a poison control center right away.
Directions
Take wipe and rub thoroughly over all surfaces of both hands
Allow hands to dry
Dispose of wipe
Do not flush
Inactive Ingredients
Water, Polyoxyethlene Alkyl Ether, Propylene Glycol, Isopropyl Alcohol, Polysorbate 20, Eucalyptus Oil, 2-Bromo-2-Nitropropane-1,3-diol, Methylchloroisothiazolinone, Methylisothiazolinone
Package Label.Principal Display Panel
Image Description (Antibacterial Hand Wipes Eucalyptus)
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