Hand Sanitizer Gel
FDA Label NDC 77693-010
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 Hand Sanitizer (NDC 77693-010). 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, use, warnings, do not use, stop use and ask a doctor if:, 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 65%
Purpose
Antiseptic
Use
for hand washing to decrease bacteria on the skin.
Warnings
For external use only. Flammable, keep away from fire and flame.
Do Not Use
in the eyes.
Stop Use And Ask A Doctor If:
- Irritation and redness develop.
- Condition 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
- Wet hands thoroughly with product and allow to dry without wiping.
Other Information
- Do not store above 105°F
- may discolor some fabrics
- harmful to wood finishes & plastic
Inactive Ingredients
Carbomer, Triethanolamine, Water
Questions Or Comments
1-833-99B-SAFE. (1-833-992-7233)
Package Labeling:
Bottle (Bottle)
* Please review the disclaimer below.
