Active Ingredients
Benzalkonium Chloride, 0.13%
Antiseptic Wipe
FDA Label NDC 71310-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Taizhou Kangping Medical Science And Technology Co., Ltd. for the product Antiseptic Wipe (NDC 71310-007). 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 ingredients, purpose, uses, warnings, do not use, stop use, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For handwashing to decrease bacteria on the skin.
Warnings
For external use only.
Do Not Use
in the eyes or apply over large areas of the body.
Stop Use
if irritation, redness or other symptoms develop.
Consult a doctor if the condition persists or gets worse.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Open packet, unfold and use as a washcloth.
Other Information
Store at room temperature: 15°-30°C (59°-86°F)
Inactive Ingredients
Purified water
Other
BZK ANTISEPTIC WIPE
• Apply topically as needed
• Sterile unless pouch is opened or damaged
For External Use Only
Package Label.Principal Display Panel
Image Of Pouch Label (Urg Bzk Single)
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