Hand Sanitizer Gel
FDA Label NDC 47682-511

13 label sections · Submitted to the FDA by Unifirst First Aid Corporation · 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, 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.

Other

Drug Facts

Otc - Active Ingredient

Active ingredient

Ethyl Alcohol 66.5%

Otc - Purpose

Purpose

Antiseptic

Indications & Usage

Uses

  • for handwashing to reduce bacteria on skinwithout soap and water
  • recommended for repeated use

Warnings

Warnings

Flammable. keep away from fire of flame.

For external use only.

Otc - Stop Use

Stop use and ask doctor if irritation and redness develops and persists for 72 hours

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If ingested, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions

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

Inactive Ingredient

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

Medi-First Antiseptic Bio-Hand Cleaner Label

MEDI-FIRST®

Antiseptic Bio Hand Cleaner

Ethyl Alcohol 66.5%

Instant Hand Sanitizer

with Aloe Vera

Mfd. for Medique Products

Fort Myers, FL 33967

Product # 51173

0.0570 fl. oz. (1.68 ml) Packets

25 per box

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