Otc - Active Ingredient
Active Ingredient Ethyl Alcohol 52.0%
Hand Sanitizer
FDA Label NDC 29500-910
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Personal Care Products for the product Hand Sanitizer (NDC 29500-910). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose Antimicrobial
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.
Indications & Usage
Uses hand sanitizer to help reduce bacteria on the skin.
Warnings
Warnings
For external use only.
Flammable. Keep away from heat and flame.
When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.
Stop use and ask a doctor if irritation or redness develops.
Dosage & Administration
Directions
Wet hands thoroughly with product and rub into skin until dry
Children under 6 years of age should be supervised by an adult when using this product.
Inactive Ingredient
Inactive Ingredients
Aloe barbadensis leaf juice, carboner, fragrance, glycerin, propylene glycol, tocephenyl acetate (Vitamin E), triethanomolamine, water (aqua)
Package Label.Principal Display Panel
Label (Twelveozhs)
Personal Care
Kills 99.9% of germs*
Hand Sanitizer
Antibacterial with Moisturizers and Vitamin E
12 fl oz. (355 ml)
* Please review the disclaimer below.
