Antiseptic Wipe Solution
FDA Label NDC 72459-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yiwu Ori-power Medtech Co.,ltd. for the product Antiseptic Wipe (NDC 72459-015). 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 ingredients, purpose, inactive ingredients, use, directions, storage, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Benzalkonium Chloride 0.13%
Purpose
First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.
Inactive Ingredients
Purfied water, Sodium Bicarbonate
Use
Sanitize hands Clean wounds
Directions
Tear open packet, unfold towelette, use to cleanse desired skin area. Discard towelette appropriately after use.
Storage
Store at room temperature 15°C - 30°C (59°F - 86°F).
Warnings
Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If pain, irritation, redness, swelling, or infection develops, discontinue use and consult physician.
Keep Out Of Reach Of Children
In case of accidental swallowing, seek medical help and contact poison control imeediately
Package Labeling:
Label (Label)
* Please review the disclaimer below.
