Active Ingredient
Benzalkonium Chloride, 0.15% w/w;
Didecyldimonium Chloride, 0.2% w/w;
Ethanol Alcohol, 15% w/w.
Alcohol Wipes
FDA Label NDC 75543-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Fujian Yifa Healthcare Products Co., Ltd. for the product Alcohol Wipes (NDC 75543-101). 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, inactive ingredient, purpose, when using, do not use, stop use, keep out of reach of children, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Phenoxyethanol, Propylene Glycol, Glycerin, Water.
Purpose
Sterilization.
When Using
Skin’s cleaning care, Article surface’s cleaning and maintenance.
Do Not Use
- on children less than 2 months of age
- on open skin wounds
Stop Use
Discontinue use if allergic reactions occur.
Keep Out Of Reach Of Children
Keep out of reach of children.
Indications & Usage
Skin’s cleaning care, Article surface’s cleaning and maintenance.
Remove seal, pull out sheet and wipe skin or articles.
(For external use only)
Dosage & Administration
Use it as needed, after following the usage instructions.
For external use only.
Warnings
This product is disposable and should not be reused.
Check whether the package is in good condition before use. If the package is found to be untidy, it is not suitable for use.
Package Label. Principal Display Panel
101 (101)
* Please review the disclaimer below.
