Janitex Antibacterial Wet Wipes
FDA Label NDC 79519-021
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pacific Health Systems Inc. for the product Janitex Antibacterial Wet Wipes (NDC 79519-021). 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, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.1 %
Purpose
Antiseptic Hand Cleanser
Uses
Kills harmful germs
Warnings
• For external use only. Harmful if swallowed.
• When using this product, avoid contact with the eyes. If contact occurs, rinse thoroughly with water.
• Stop use and ask a doctor if irritation develops.
Otc - Keep Out Of Reach Of Children
• Keep out of reach of children. If swallowed, call a poison control center or get medical help right away.
Directions
• Adults and children over 2 years old
• For occasional and personal domestic use
• Supervise children when they use this product
• Rub thoroughly into hands for at least 30 seconds. Allow to dry
Inactive Ingredients
Aqua, Sodium Benzoate, Phenoxyethanol, Parfum, Benzoic Acid, Dehydroacetic Acid, Panthenol, Sodium Cocoamphoacetate, Sodium Lauriminodipropionate, Octyldodecanol
Other Informations
Store in a cool & dry place
Questions?
+1 (862) 318-4763
Packaging
Image (79519021 01)
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