Hand Sanitizer Gel
FDA Label NDC 47682-511

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Unifirst First Aid Corporation for the product Hand Sanitizer (NDC 47682-511). 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, active ingredient, purpose, uses, warnings, do not use, stop use and ask doctor if, 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

Drug Facts

Active Ingredient

Ethyl Alcohol 66.5%

Purpose

Antiseptic

Uses

  • for handwashing to reduce bacteria on skin whenever soap and water are not available
  • reduces bacteria that potentially can cause disease or infection
  • recommended for repeated use

Warnings

Flammable. keep away from fire of flame.

For external use only.

Stop Use And Ask Doctor If

  • irritation and redness develops and persist for 72 hours.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • wet hands thoroughly with product and allow to dry without wiping
  • children under 6 years of age should be supervised when using this product

Inactive Ingredients

aloe vera, carbomer, DD&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

Principal Display Panel – Medi-First Antiseptic Bio-Hand Cleaner

DC# 47682-511-73

MEDI-FIRST

Antiseptic Bio Hand Cleaner

Instant Hand Sanitizer

with Aloe Vera

0.0570 fl. oz. (1.68 ml) Packets

25 per box

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