Active Ingredient
Benzalkonium Chloride, 0.1%
Wipe N Go
FDA Label NDC 69538-200
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Canadia Usa Corporation for the product Wipe N Go (NDC 69538-200). 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, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
Antibacterial wipes for the 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 24 hours.
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 Ingredients:
Water, Disodium EDTA, Phenoxyethanol, Glycine, Polysorbate 20, Glycerin, Fragrance, Polyaminopropyl Biguanide, Sodium Citrate
Principal Display Panel
wipe n' go
Antibacterial HAND WIPES
Made in China
Distributed by: Canadia USA Corporation.
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