Hand Sanitizer Wipe 75%
FDA Label NDC 80066-663
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pharmaxx, Inc. for the product Hand Sanitizer Wipe 75% (NDC 80066-663). 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 ingredient: [s], purpose, use[s], warnings:, do not use, when using this product, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient: [S]
Alcohol 75% (v/v)
Purpose
Antiseptic
Use[S]
Alcohol Sanitizer Wipe to help reduce bacteria/germs that potentially can cause disease.
Warnings:
For external use only. Flammable. Keep away from heat or flame
Do Not Use
- In children less than 2 months of age
- on open skin wounds
When Using This Product
keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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.
Directions
- Open bag and use for hands.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F )
Inactive Ingredients
glycerin, hydrogen peroxide, purified water USP
Package Labeling:
Bottle2 (Bottle2)
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