Dosage & Administration
store between 15-30°C(59-86°F),avoid freezing and excessive heat above 40°C(104°F)
Alcohol Wipes
FDA Label NDC 41546-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Huanghua Biological Technology Co., Ltd for the product Alcohol Wipes (NDC 41546-009). 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, inactive ingredient, indications & usage, otc - active ingredient, otc - keep out of reach of children, otc - purpose, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
pure water
Indications & Usage
1.Open cover and remove seal.
2.Pull out wipe corner from center of the roll.
3.Thread through hole in the cover.
4.Close lid after use to retain moisture.
Otc - Active Ingredient
alcohol
Benzalkamine
2-methyl-4-isothiazoline-3-one
propylene glyco
2-phenoxyethanol
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Purpose
Disinfection
Sterilization
No Rinseing
Warnings
For external use only. Flammable. Keep away from heat or flame.
Package Label.Principal Display Panel
Label (Label)
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