Active Ingredient(S)
Alcohol 75% v/v. Purpose: Antiseptic
Besafe Hand Sanitizer
FDA Label NDC 77693-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Besafe Industries Llc for the product Besafe Hand Sanitizer (NDC 77693-001). 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(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach 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
For hand washing to decrease bacterial on the skin
Warnings
For external use only. Flammable. Keep away from fire and flame.
Otc - When Using
Do not use in the eyes
Otc - Stop Use
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more then 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wet hands thoroughly with product and allow to dry without wiping
For children under 6, use only under adults supervision
Not reommended for infants
Other Information
Do not store above 105F
May discolor some fabrics
Harmful to wood finishes and plastics
Inactive Ingredients
Water, carbomer, triethanolamine, glycerin, aloe barbadensis gel, propylene glycol, tocopheryl acetate (Vitamin E)
Package Label.Principal Display Panel
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