Active Ingredients
Ethyl Alcohol 75%
Ultra Defense Advanced Hand Sanitizer
FDA Label NDC 77618-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Republic Nail, S.a. De C.v. for the product Ultra Defense Advanced Hand Sanitizer (NDC 77618-001). 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 ingredients, purpose, uses, warnings, do not use, when using this product,, 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
Purpose
Antiseptic
Uses
- hand sanitizer to help decrease baceteria on the skin
- when water, soap & towel are not available
- recommended for repetaed use
Warnings
For external use only.
Flammable, Keep away from fire or flame.
Do not apply around eyes.
Do Not Use
in ears & mouth
When Using This Product,
avoid contact with eyes. In case of contact flush eyes with water.
Stop Use And Ask A Doctor If
redness or irritation develop and persist for more than 72 hours.
Keep Out Of Reach Of Children.
Children must be supervised in use of this product.
Directions
- pump as needed into your palms and thoroughly spread on both hands.
- rub into skin until dry.
Other Informaton
- store at 20° C (68° to 77° F)
- may discolor fabrics.
Inactive Ingredients
water, glycerin, carbomer, Treithanolamine.
Package Labeling:
Label (Label)
* Please review the disclaimer below.
