Active Ingredient
Ethy Alcohol 66% v/v
First Safety Hand Sanitizing Tissue
FDA Label NDC 79984-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bonitolab Co. for the product First Safety Hand Sanitizing Tissue (NDC 79984-010). 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, Glycerin, Citric Acid
Purpose
Antiseptic
Warnings
For external use only. Flammable. Keep away from heat or flame
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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
Directions
■ Tear open packet, remove wipe
■ thoroughly wipes hands with cloth
■ Supervise children under 6 years of age when using this product
Other Information
■ Storage in a cool, dry place, Avoid freezing and excessive heat above 40 ℃ (104 ℉)
■ may discolor certain fabrics or surfaces
* Please review the disclaimer below.
