Otc - Active Ingredient
Benzalkonium Chloride - 0.13%
Antibacterial
FDA Label NDC 50157-508
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 Antibacterial (NDC 50157-508). 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, warnings, otc - stop use, otc - when using, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose - Antiseptic Skin cleanser
Indications & Usage
Uses for handwashing or decrease bacteria to the skin
Warnings
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
Dosage & Administration
Directions
- wet hands
- apply palmful to hands
- scrub thoroughly
- rinse
- For occasional and personal domestic use
- Supervise children when they use this product.
Inactive Ingredient
Lauramidopropylamine oxide, lauryl glucoside, PEG-150 distearate, glycol stearate, perfume, PEG-7 glycerly cocoate, centrimonium chloride, Citric Acid, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone,
Package Label.Principal Display Panel
2 (2)
1 (1)
3 (3)
Soap1 (Soap1)
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