Bioss Hand Sanitizer
FDA Label NDC 77134-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bioss Inc. for the product Bioss Hand Sanitizer (NDC 77134-000). 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 consult a health care practitioner if, keep out of reach of children, direction, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Ethyl alcohol 75%

Purpose

Antiseptic skin cleanser

Uses

Effective in killing bacteria (harmful) to provide an antiseptic cleaning. For personal hand hygiene to prevent the spread of bacteria.

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When Using This Product

avoid contact with eyes. In case of contact, immediately flush eyes with water.

Stop Use And Consult A Health Care Practitioner If

irritation or redness develops.

Keep Out Of Reach Of Children

Do not use on children/infants under 2 years old (except on the advice of a doctor).

Direction

For occasional use for personal household use. Rub well for at least 30 seconds. Let dry.

Other Information

Store at 20°C (68° to 77°F) cool place.

Inactive Ingredients

Acrylates/c10-30, Alkyl Acrylate Crosspolymer, Triethanolamine, Citrus Aurantium Bergamia (Bergamot) Fruit Extract, Lemon oil. 

Questions?

1-866-795-8481

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

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