Label: TAVOS HAND SANITIZER GEL- isopropyl alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 22, 2022

If you are a consumer or patient please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION
    This is a hand sanitizer manufactured according to the - Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19) ...
  • Active Ingredient(s)
    Isopropyl Alcohol 72% v/v. Purpose: Antiseptic
  • Purpose
    Antiseptic, Hand Sanitizer
  • Use
    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
    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 ...
  • STOP USE
    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
    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 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)
  • Inactive ingredients
    carbopol, glycerin, aminomethylpropanol, distilled water
  • Package Label - Principal Display Panel
    187.5 ml NDC: 80234-9009-02 - 50 ml NDC: 80234-9009-03 - 250 ml NDC: 80234-9009-04 - 250 ml NDC: 80234-9009-05 - 250 ml NDC: 80234-9009-06 - 250 ml NDC: 80234-9009-07
  • INGREDIENTS AND APPEARANCE
    Product Information
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!