Active Ingredient
Benzalkonium Chloride 0.13%
Wipe Out Fresh Scent Antibacterial
FDA Label NDC 77878-017
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tzumi Innovations Llc for the product Wipe Out Fresh Scent Antibacterial (NDC 77878-017). 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, purpose, use, warnings, otc - stop use, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Use
■ To decrease bacteria on the skin that could cause disease
Warnings
For external use only. Flammable.
When using this product,
keep out of eyes. In case of contact with eyes, flush thoroughly with water
Avoid contact with broken skin
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
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
Directions
Hold can upright 6"-8" from hand.
Spray 3-4 seconds until covered with mist
For children under 6, use only under adult supervision
Not recommended for infants
Other Information
Contents under pressure
Keep away from heat, sparkles, and open flame
Do not puncture or incinerate container
keep in dry, cool and well ventilated place
Recommended storage temperature: 32F-104F (0-40C)
Inactive Ingredients
Aloe Barbadensis Leaf Etract, Fragrance, Glycerin, Phenoxyethanol, Tocopheryl Acetate, Water
Package Label.Principal Display Panel
Image Description (Img 5775 2)
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