Wet Wipes Antibacterial Travel Pack Cloth
FDA Label NDC 52862-656
11 label sections · Submitted to the FDA by International Wholesale, Inc. · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by International Wholesale, Inc. for the product Wet Wipes Antibacterial Travel Pack (NDC 52862-656). 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 drug facts, active ingredient (by weight), purpose, uses, warnings, do not use:, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient (By Weight)
Benzalkonium Chloride 0.13%
Purpose
Antibacterial
Uses
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.
For children under 2 years ask a doctor before use. For children use under adult supervision.
Directions
Do not expose to direct sunlight, preferably place them in a cool place. Do not use on furniture. Do not flush down toilets, dispose in trash recepticals.
Peel back the resealable label and remove a wipe. Wipe the hands and allow it to dry. Reseal after use to prevent the wipes from drying out.
Inactive Ingredients
Aqua, Phenoxyethanol, Propylene Glycol, Polysorbate 20, Aloe Barbadensis Leaf Extract, Polyaminopropyl Biguanide, PEG-7 Glyceryl Cocoate, PEG-40 Hydrogenated Castor Oil, Parfum, Tocopheryl Acetate.
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