Active Ingredient
Ethyl Alcohol 75% v/v
Alcohol Wipes Patch
FDA Label NDC 77412-199
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shandong Liaocheng Chaoyue Daily Necessities Co., Ltd. for the product Alcohol Wipes (NDC 77412-199). 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 active ingredient, purpose, use, warnings, when using this product:, stop use and ask a doctor if, keep out ofreach of children, directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
To help reduce bacteria that potentially can cause disease
Warnings
For external use only; hands, general cleansing.
Does not replace wipes used for medical procedures.
Flammable； keep away from fire or flame.
Do not ingest.
When Using This Product:
Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Avoid contact with broken skin.
Stop Use And Ask A Doctor If
lrritation and redness develop.
Condition persists for more than 72 hours.
Keep Out Ofreach Of Children
If swallowed, get medical help or contact a poison control center right away.
Directions:
Single use wipes for hands.
Close properly after dispensing to maintain purity,as alcohol by its nature evaporates quickly.
Dispose of properly.
DO NOT FLUSH.
Apply thoroughly to hands to cover all surfaces. Rub hands together until dry.
Other Information
Keep out of light; store at room temperature 59°F-86°F
Inactive Ingredients:
Glycerol, Water.
* Please review the disclaimer below.
