Active Ingredient
Active Ingredient
Benzethonium Chloride 0.3%
Wet Wipes Antibacterial Hand Wipes
FDA Label NDC 77125-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo�yinzhou Greenlight�international�trade Co.,ltd for the product Wet Wipes Antibacterial Hand Wipes (NDC 77125-003). 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, do not use, when using this product, stop use and ask a doctor, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Purpose Antimicrobial
Use
Use
Decrease bacteria on skin
Warnings
For External use only
Do Not Use
Do not use if you are allergic to any of the ingredients
When Using This Product
When using this product do not get into eyes, if contact occurs rinse thoughly with water
Stop Use And Ask A Doctor
Stop use and ask a doctor if irritation or rash develops and continues for more then 72 hours
Keep Out Of Reach Of Children
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center
Directions
Directions
Adults and children 2 years and over
- apply to hands
- allow to dry without wiping
- Children under 2 years ask a doctor before use
Other Information
Other information
- store at room temperature
- may discolor certain fabrics
Inactive Ingredients
Inactive Ingredients
water, propylene gylcol, gylcerin, PEG-40 hydrogenated castor oil, disodium EDTA, aloe barbadnsis leaf juice, methylparaben, propylparaben
Package Label
32 wipes NDC 77125-003-01
Wet Wipes Label (Wetwipes)
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