Virocide Hand Sanitizer Eucalyptus
FDA Label NDC 77005-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Virocide Llc for the product Virocide Hand Sanitizer Eucalyptus (NDC 77005-004). 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 other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - stop use, otc - 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

→ Other

→ Otc - Active Ingredient

→ Otc - Purpose

→ Indications & Usage

→ Warnings

→ Otc - Do Not Use

→ Otc - Stop Use

→ Otc - Keep Out Of Reach Of Children

→ Dosage & Administration

→ Other Safety Information

→ Inactive Ingredient

→ Package Label.principal Display Panel

Other

DRUG FACTS

Otc - Active Ingredient

ACTIVE INGREDIENT[S]
Ethyl Alcohol (70%) v/v

Otc - Purpose

PURPOSE
Antiseptic

Indications & Usage

USE(S)
Hand sanitizer to help reduce bacteria that
potentially can cause disease. For use when soap
and water are not available.

Warnings

WARNINCS
For external use only. Keep away from heat
or flame

Otc - Do Not Use

DO NOT USE
·in children less than 2 months of age
·on open skin wounds

Otc - Stop Use

Stop use and ask a doctor
if rash or irritation occurs. These may be signs of a
serious condition

Otc - 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.

Dosage & Administration

DIRECTIONS
Place enough 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