Active Ingredient
Benzalkonium Chloride .13%.
Alby
FDA Label NDC 80686-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by K-zoe Marketing for the product Alby (NDC 80686-001). 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, purpuse, uses, warnings, otc - keep out of reach of children, instructions, other info, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpuse
Antiseptic.
Uses
For areas and surfaces to decrease bacteria and germs.
Warnings
For external use only. Keep away from heat or flame.
Avoid contact with eyes
If swallowed get medical attention right away.
Otc - Keep Out Of Reach Of Children
Keep away from children
Instructions
Apply directly over surface, let it dry.
Other Info
Store between 15° - 30°C (59°F - 86°F). Avoid freezing and excessive heat above 40°C (104°F).
Inactive Ingredients
Water, glycerin, fragance.
Don´T Use
Don´t use in children less than 2 months of age. On open skin wounds.
Indications & Usage
Spray Sanitizer
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