Active Ingredients
Ethyl alcohol 70% v/v
Nuuxsan Instant Hand Sanitizer
FDA Label NDC 72758-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Albek De Mexico, S.a. De C.v. for the product Nuuxsan Instant Hand Sanitizer (NDC 72758-003). 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, stop use and ask a doctor if, keep out of reach of children., directions, 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 bacteria on the skin
- when water, soap & towel are not aviable recommended for repeated use.
Warnings
For external use only.
Flammable. Keep away from fire or flame.
Do not apply arround eyes.
Do Not Use
in ears & mouth
Stop Use And Ask A Doctor If
ittitation and redness develop and persist for more than 72 hours.
Keep Out Of Reach Of Children.
Children must be supervised in use of this product.
Directions
- use as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.
Other Information
- Shore al 20°C (68° to 77°F).
- May discolor fabrics.
Inactive Ingredients:
water, carbomer, triethnolamine, glycerin, propylene glycol, fragrance, aloe barbadensis leaf juice.
Package Labeling:100 Ml
Label (Label)
Package Labeling:500 Ml
Label2 (Label2)
* Please review the disclaimer below.
