Active Ingredient
Benzalkonium Chloride 0.2%
Goodday Clean Wet Wipes
FDA Label NDC 79907-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Maxkorea Co., Ltd. for the product Goodday Clean Wet Wipes (NDC 79907-010). 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 ingredients, purpose, warnings, keep out of reach of children, uses, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredients
Water, Sodium hydroxide, Glycerin, Yellow 4, Blue 1
Purpose
Antiseptic
Warnings
For external use only
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Do not use
■ on infants
■ on open skin wounds
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When using this product
■ avoid getting into the eyes
■ In case of eye contact immediately flush eyes thoroughly with water
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Stop use and ask a doctor
■ if irritation or redness develops
■ conditions persist for more than 72 hours
■ redness is present
Keep Out Of Reach Of Children
■ in case of accidental ingestion, contact a doctor or Poison Center immediately
Uses
■ hand sanitizing wipes to help reduce bacteria on the skin. For use when soap and water not available
Directions
■ thoroughly wipes hands with cloth
■ rub hands together until dry
Other Information
■ Storage in a cool, dry place, Avoid freezing and excessive heat above 30 ℃ (86 ℉)
■ Do not flush
* Please review the disclaimer below.
