Active Ingredient
Alcohol 63%
Hand Sanitizer
FDA Label NDC 70939-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dongguang Shuoguo Silicone Products Co., Ltd. for the product Hand Sanitizer (NDC 70939-001). 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, purpose, use, warnings, keep out of reach of children, directions, 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
Purpose
Antiseptic Hand Sanitizer
Use
to decrease bacteria on the skin
Warnings
For external use only
Flammable: Keep away from fire or flame
Alcohol is used
Do not use in the eyes. If this happens, rinse thoroughly with water.
In case of deep or puncture wounds, consult your doctor
Stop use and ask a doctor if irritation or redness develops and persists for more than 72 hours
Keep Out Of Reach Of Children
if swallowed
get medical help or contact a Poison Control Center right away.
Directions
Liberally spray on skin and gently massage until absorbed
Inactive Ingredient
Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadenis Leaf, Fragrance, Carbomer
Package Label.Principal Display Panel
Label (Label)
* Please review the disclaimer below.
