Active Ingredient (In Each Wipe)
Benzalkonium Chloride 0.13% Purpose: Antiseptic
Push Clean
FDA Label NDC 73737-436
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pushclean Technology Plastik Sanayi Ve Ticaret Limited Sirketi for the product Push Clean (NDC 73737-436). 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 (in each wipe), purpose, use[s], warnings, do not use, stop use and ask a doctor, 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
Use[S]
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Stop Use And Ask A Doctor
if irritation or rash occurs. These may be signs of a serious condition.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
- Place the container on a hard flat surface. Using your thumb, press and hold firmly in the center of the container for a second and release. Wait for the towelette to rise completely out of the container. Remove and unfold the towelette for use.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
- Avoid freezing and excessive heat above 40C (104F)
- Store between 20-25 C (68-77F)
Inactive Ingredients
sodium hydroxide, water
Package Label.Principal Display Panel
73737-436-24
24 Pack
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