Hand Sanitizer Alcohol Hand Gel
FDA Label NDC 76892-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Design International Group for the product Hand Sanitizer Alcohol Hand (NDC 76892-001). 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 ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of childre., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Alcohol 75%
Purpose
Antiseptic
Use
for hand-washing to decrease bacteria on the skin,only when water is available
Warnings
Flammable, keep away from fire and flames
For external use only
When Using This Product
- do not get into eyes.
- if contact occurs, rinse eyes thoroughly with water
Stop Use And Ask A Doctor If
- irritation and redness develop
Keep Out Of Reach Of Childre.
- 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
Inactive Ingredients
Water, Glycerin, Carbomer,Triethanolamine.
Package Labeling: 1000Ml
Label (Label)
Package Labeling:500Ml
Bottle (Bottle)
* Please review the disclaimer below.
