Hand Sanitizer
FDA Label NDC 77811-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aventi Medical, Llc for the product Hand Sanitizer (NDC 77811-001). 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 drug facts, active ingredients, purpose, uses, warnings, when using this product, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Ethyl Alcohol 70%
Purpose
Antiseptic
Uses
For handwashing to decrease bacteria on the skin.
Warnings
Flammable. Keep away from fire or flame. For external use only.
When Using This Product
Do not use in eyes. In case of contact with eyes, rinse with water.
Stop Use And Ask A Doctor
if irritation and redness develop and persist.
Keep Out Of Reach Of Children.
If swallowed, get medical help promptly.
Directions
Wet hands thoroughly with product and allow to dry without wiping.
Other Information
Store under 105 oF
Inactive Ingredients
Aloe Barbadensis Leaf, Carbomer, Dimethicone, Triisopropanolamine, Water
Package Labeling: 1000L, 77811-001-01
1000 (1000l)
Package Labeling: 3785Ml, 77811-001-02
3785 (3785ml)
* Please review the disclaimer below.
