Sani T Hand Sanitizer
FDA Label NDC 79410-002

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Corporativo Cubrete, S.a. De C.v. for the product Sani T Hand Sanitizer (NDC 79410-002). 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, purpose, uses, warnings, when using this product, stop use and ask a doctor, 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

Active Ingredient

Ethyl alcohol 80% v/v

Purpose

Antimicrobial

Uses

  • Hand Sanitizer to help reduce bacteria that potentially cause disease.
  • For use when soap and water are not available.

Warnings

Flammable

  • Keek away from fire or flame
  • For external use only.

When Using This Product

  • Do not use it in or near the eyes
  • In case of contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor

if skin irritation occurs.

Keep Out Of Reach Of Children.

If swallowed, ger medical help in a PoisonControl Center immediately.

Directions

  • Put enough product in your palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product.

Other Information

  • Store below 110° F (43°C)
  • May discolor certain fabrics

Inactive Ingredients

Triethanolamine, Carbomer, Polysorbate, Water, Glycerin.

79410-002-01

Bottle (Bottle)

Bottle (Bottle)

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