Active Ingredient(S)
Alcohol 75% v/v
Belar Hand Sanitizer
FDA Label NDC 79716-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Laboratorios Belar S.a. De C.v. for the product Belar Hand Sanitizer (NDC 79716-001). 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 ingredient(s), purpose, use(s), 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
Use(S)
This product does not replace the use of soap and water, Recommended for repeated use.
Warnings
For external use only. Flammable. Keep away heat.
Do Not Use
- In children less tan 2 months of age
- An open skin wound
When Using This Product
keep out 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
- Rub hands together briskly for at least 30 seconds until dry.
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients:
Distilled Water, Propylene Glycol, Carbopol, Triethanolamine.
Package Labeling:
Label (Label)
* Please review the disclaimer below.
