Active Ingredient
Benzalkonium Chloride 0.13%
Wet Wipe
FDA Label NDC 80332-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Quzhou Zefeng Import& Export Co., Ltd. for the product Wet Wipe (NDC 80332-001). 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
Antimicrobial
Use
For hand washing to decrease bacteria on the skin.
Recommended for repeated use.
Warning
For external use only
When using this product, avoid contact with the eyes.
In case of contact, flush eyes thoroughly with water.
Stop use and ask a doctor if irritation and redness develop.
Otc - 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
For hand sanitizing to decrease bacteria on the skin.
Recommended for repeated use.
Inactive Ingredients
Aqua, Propylene Glycol, Polysorbate 20, Phenoxyethanol.
Package Label.Principal Display Panel
75 PCS NDC 80332-001-01
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