Otc - Active Ingredient
Active Ingredient: Ethyl Alcohol 70% v/v
Alcohol Wipes
FDA Label NDC 74835-012
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hangzhou Lookon Commodity Co., Ltd. for the product Alcohol Wipes (NDC 74835-012). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose:Antiseptic
Indications & Usage
Uses: to decrease bacteria on the skin
Warnings
Warnings:
For external use only
Flammable: Keep away from flame or high heat.
When use this product avoid contact with the eyes,face and broken skin.
Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.
Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center right away.
Otc - When Using
When use this product avoid contact with the eyes,face and broken skin.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center right away.
Storage And Handling
Note: Do not store above 100℉. Non-staining may discolor some fabrics.
Dosage & Administration
Directions:
Rub wipe thoroughly over all surfaces of both hands
Allow to dry without wiping
Supervise children under 6 years old
Not recommended for infants
Dispose of wipes in trash after use. Do not flush.
Inactive Ingredient
Inactive Ingredient:
Aqua,Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Juice, Decyl Glucoside
Package Label.Principal Display Panel
NDC：74835-012-01
NDC：74835-012-02
NDC：74835-012-03
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