Active Ingredient
Benzalkonium chloride 0.115%
Antibacterial Wet Wipes
FDA Label NDC 59575-501
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hebei Yihoucheng Commodity Co.,ltd. for the product Antibacterial Wet Wipes (NDC 59575-501). 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, 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
Antibacterial
Use
Decreases bacteria on skin
Warnings
For external use only.
Do not use over large areas of the body
if you are allergic to any of the ingredients.
When using this product do not get into eyes.
If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash
develops and continues for more than 72 hours.
Keep out of reach of children.
If swallowed, get medical help or contact
a Poison Control Center right away.
Keep Out Of Reach Of Children
if swallowed
get medical help or contact a Poison Control Center right away.
Directions
For adults and children of 2 years and over use
on hands and face to clean and refresh, allow
skin to air dry.
For children under 2 years ask a doctor before use.
Inactive Ingredient
Water,SD Alcohol 40,Propylene Glycol,Aloe Barbadensis Leaf,Potassium sorbate,Tocopherol,Quaternium 52,PEG-60 Lanolin,Citric Acid,Disodium EDTA
Package Label.Principal Display Panel
1 (Sku187422 Box Bvtest Jul25rev)
3 (Sku187423 Rev Jul15rev Ol)
2 (Sku187422 Bvtest Jul25rev)
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