Active Ingredient
Benzalkonium Chloride, 0.13%
Antiseptic Wipe
FDA Label NDC 55550-210
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Total Resources for the product Antiseptic Wipe (NDC 55550-210). 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, stop use if, 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
First Aid Antiseptic
Use
Antiseptic cleansing of face, hands and body without the use of soap and water. Air dries in seconds.
Warnings
Do not use in the eyes or apply over large areas of the body.
Stop Use If
irritation, redness or other symptoms develop. Cosult a doctor if the condition persists or worsens.
Otc - Keep Out Of Reach Of Children
If swallowed, seek medical help or contact a Poison Control Center immediately.
Directions
Tear open packet, unfold, and use as a washcloth.
Other Information
Store at room temperature 59° - 86°F (15° - 30°C)
Inactive Ingredient
water
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