Otc - Active Ingredient
Benzalkonium Chloride - 0.13%
Moonlite Antibacterial
FDA Label NDC 50157-511
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 Moonlite Antibacterial (NDC 50157-511). 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 - Antiseptique(skin)cleanser
Indications & Usage
Uses Effective in destorying(harmful) bacteria to provide antiseptic cleansing.
Warnings
Warning For external use only
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops
Otc - When Using
When using the product
- avoid contact wiith 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
Direction
- Adults and children over 2 year
- For occasional and personal domestic use
- Supervise children when use this product
- Lather in hands with water for at least 30 seconds
- Rinse well
Other Safety Information
- Store below 110F(43)
- May discolor certain fabrics or surfaces.
Inactive Ingredient
Water,Lauramidopropylamine Oxide ( Triaminox LO ), Lauryl Glucoside, Citric Acid, PEG-150 distearate, Glycol Stearate, PEG-7 Glyceryl Cocoate,Cetrimonium Chloride, Tetrasodium EDTA,Isopropyl myristate, Aloe Leaf, Tocopheryl Acetate, Methylchloroisothiazolinone, Methylisothiazolinone,
Package Label.Principal Display Panel
1 (1)
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