Antibacterial Hand Sanitizer Gel
FDA Label NDC 71513-105

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Broder Bros Co. for the product Antibacterial Hand Sanitizer (NDC 71513-105). 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 ask a doctor, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

For hand sanitizing

Warnings

Flammable. Keep away from heat and flame.

For external use only

When Using This Product

  • Keep out of eyes
  • In case of contact with eyes, flush thoroughly with water
  • Avoid contact with broken skin
  • Do not inhale or ingest

Stop Use And Ask A Doctor

if irritation and redness develops and persists for more than 72 hours

Keep Out Of Reach Of Children

if swallowed, get medical help promptly and contact Poison Control

Directions

  • Wet hands thoroughly with product, briskly rub together until dry
  • Always supervise children in the use of this product
  • Children under 6 months of age: ask a doctor

Other Information

Store at 20° C (68° to 77°F)

Inactive Ingredients

Carbomer, fragrance, glycerin, propylene glycol, tocopheryl acetate, triethanolamine, water

Questions?

1-800-873-7746 M-F 8am - 5pm EST

Other

0.5 oz / 15 ml

Dist. By: Broder Bros. Co., dba Prime Line

Gaffney, SC 29341

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