Otc - Active Ingredient
Benzalkonium Chloride - 0.13%
Everwipe Antibacterial
FDA Label NDC 50157-264
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Brands International Corporation for the product Everwipe Antibacterial (NDC 50157-264). 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 otc - active ingredient, otc - purpose, indications & usage, dosage & administration, warnings, otc - stop use, otc - when using, otc - 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
Otc - Purpose
Purpose: Antibacterial
Indications & Usage
Effective in destroying bacteria to provide antiseptic cleaning.
Dosage & Administration
Direction
- wet hands
- apply palmful to hands
- scrub thoroughly
- rinse
Warnings
For external use only
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops
Otc - When Using
When using this product
- do not get it into eyes. If contact occurs, rinse eye thoroughly with water
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
Inactive Ingredient
Lauramidopropylamine oxide, Lauryl glucoside, PEG-150 distearate, Glycol Stearate, Perfume, Aloe extract, Tocopheryl Acetate, Peg 7- Glyceryl Cocoate, Cetrimonium, Chloride, Citric Acid, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone.
Package Label.Principal Display Panel
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