Active Ingredient
Benzalkonium Chloride, 0.10%
Aerowipe Swab
FDA Label NDC 55305-118
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aero Healthcare for the product Aerowipe (NDC 55305-118). 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:, do not use:, stop use and ask a doctor if:, 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
First Aid Antiseptic
Use
To prevent infection in minor cuts, scrapes and burns
Warnings:
For external use only
Do Not Use:
- For deep puncture wounds, animal bites, or serious burns
- In eyes or over large area of the body
Stop Use And Ask A Doctor If:
- Irritation, redness, or symptoms develop
- 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:
Tear pouch and clean the affected area.
Inactive Ingredient
Purified Water
Package Label
AEROWIPE Antiseptic Wipe
Contains: Benzalkonium Chloride
Code: AW8001
1 Wipe
Manufactured for Aero Healthcare
AUS - Armidale NSW 2350
UK - Horsham RH13 5QL
US - Congers NY 10920
www.aerohealthcare.com
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