Antibacterial Hand Sanitizer
FDA Label NDC 77879-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bt Supplies West Inc for the product Antibacterial Hand Sanitizer (NDC 77879-001). 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 drug facts, active ingredient, purpose, use:, warnings:, 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

Drug Facts

Active Ingredient

Ethyl Alcohol 73% v/v

Purpose

Antimicrobial

Use:

Hand sanitizer to help reduce bacteria on skin.

Warnings:

Flammable. Keep away from fire or flame.
For external use only.

When Using This Product

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

Stop Use And Ask A Doctor

if irritation or rash appears and lasts.

Keep Out Of Reach Of Children.

if swallowed, get medical help or contact a Poison Control 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

Other Information:

Store below 110°F (43°C)

Inactive Ingredients:

Deionized Water, Glycerol, Carbopol, Triethanolamine

Package Labeling: 250Ml

Label (Label)

Label (Label)

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