Active Ingredient
Ethyl alcohol 75%
Cb Advanced Hand Sanitizer
FDA Label NDC 76813-014
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cb Distributors, Inc. for the product Cb Advanced Hand Sanitizer (NDC 76813-014). 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, when using this product, stop use and ask a doctor if, 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
• to help reduce bacteria on the skin.
Warnings
For external use only
Flammable. Keep away from fire or flame.
When Using This Product
do not use in or near the eyes. In case of contact, flush eyes with water.
Stop Use And Ask A Doctor If
irritation or rash appears and lasts.
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 • Children under 6, use only under adult supervision.
Other Information
• store below 105°F • may discolor certain fabrics.
Inactive Ingredients
• Purified water(Aqua), Aloe Barbadensis Leaf Extract, Acrylates/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine.
Package Labeling:
Label (Label)
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