Dosage & Administration
Remove and unfold wipe from package
Wipe hands and nails thoroughly
Allow sking to dry without wiping
Discard Properly
Single Use Only
Antiseptic Hand Wipe
FDA Label NDC 90024-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Metro Medical Equipment Mfg. Inc for the product Antiseptic Hand Wipe (NDC 90024-001). 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 dosage & administration, otc - active ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, intended use of the device, warnings, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Ethyl Alcohol 15%
Benzalkonium Chloride .1%
Indications & Usage
Hand sanitizer to help reduce bacteria on the skin.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Purpose
Antiseptic
Intended Use Of The Device
Hand sanitizer to help reduce bacteria on the skin.
Warnings
Flammable
Keep away from fire or flame
For external use only
When using this product aboid use near eyes
If contact occurs, rinse thoroughly with water
Stop use and ask a doctor if irritation or rash appears and lasts
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
Remove and unfold wipe from package
Wipe hands and nails thoroughly
Allow skin to dry without wiping
Discard properly
Single Use Only
Other
Store at room temperature
Inactive Ingredient
Propylene glycol
Phenoxyethanol
Cetylpyridinium Chloride
Water
spunlace non-woven fabric
* Please review the disclaimer below.
