Other Information
Store below 110°F (43°C)
Alcohol Wipes
FDA Label NDC 55490-030
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Baijieyuan Biotechnology (shandong) Co., Ltd. for the product Alcohol Wipes (NDC 55490-030). 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 other information, inactive ingredient, use, otc - active ingredient, otc - keep out of reach of children, otc - purpose, warnings, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Glycerol
Aloe extract
Pure water
Use
Wipe on skin to help reduce bacteria on skin that potentially can cause disease.
Otc - Active Ingredient
Ethyl alcohol
Otc - Keep Out Of Reach Of Children
Keep out of reachof children.lf swallowed, get medical help or contact a Poison Control Center right away.
Otc - Purpose
Antiseptic
Warnings
For external use only.Flammable,keep away from heat or flame.
Directions
Rub hands on wipe,and use to disnfect.
Supervise children under 6 years of age when using this product.
Otc - Do Not Use
On childiren less than 2 months of age
Otc - When Using
When using this product keep out of eyes, ears,and mouth.in case of contact witheyes, rinse eyes thorougly with water
Otc - Stop Use
Stop use and ask a doctor if iritation or rash occurs.These may be signs of a serious condition.
Package Label.Principal Display Panel
Label (Label)
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