Uses
To decrease bacteria on the skin that could cause disease
1.Remove the wipe from the center of the canister.
2.The next wipe will come out automatically.
3.Close the lid to keep the wipes moist.
Antibacterial Wipes
FDA Label NDC 92185-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hangzhou Suncilia Yuehui Biotechnology Co., Ltd for the product Antibacterial Wipes (NDC 92185-001). 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 uses, directions, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, other information, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Directions
allow to dry without wiping for children under 6, use only underadult supervision not recommended for infants
Warnings
For external use only
Otc - When Using
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 and redness developcondition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. lf swallowed, get medical help orcontact a Poison Control Center right away.
Other Information
keep containers tightly closed in a dry, cool and well-ventilated place
recommended storage temperature: 32°F to 104°F(0°C to 40°c)
Inactive Ingredient
aloe barbadensis leaf juice, fragrance, phenoxyethanol,polysorbate 20, propylene glycol, tocopheryl acetate, water
Otc - Active Ingredient
Benzalkonium Chloride 0.13%
Otc - Purpose
Disinfection
Sterilization
No Rinseing
Package Label.Principal Display Panel
Label (Label)
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