Active Ingredient[S]
Alcohol 70% v/v
Zanilast Plus
FDA Label NDC 69912-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nanomateriales Qu�micos Avanzados, S.a. De C.v. for the product Zanilast Plus (NDC 69912-008). 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 ingredient[s], purpose, uses, warnings, do not use, 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
Purpose
Antiseptic
Uses
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away from heat or flame.
Do Not Use
- In children less than 2 months of age
- On open skin wounds
When Using This Product
keep out of eyes,ears, and mouth. In case of contact with eyes,rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
if irritation or rash occurs. These may be signs of a serious condition.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Place enough product on hands to cover all surfaces. Rub hands together until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
- Store between 15-30 °C (59-85 °F)
- Avoid freezing and excessive heat above 40 °C (104°F).
Other Ingredients
Water,glycerin, triethanolamine,carbomer,fragrance,zinc oxide,zinc pyrithione.
Package Labeling:1000Ml
Label (Label)
Package Labeling:3785.41Ml
Label2 (Label2)
* Please review the disclaimer below.
