Hand Sanitizer
FDA Label NDC 55316-253

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dza Brands Llc for the product Hand Sanitizer (NDC 55316-253). 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 using 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 65%

Purpose

Antiseptic

Uses

  • to help reduce bacteria on the skin

Warnings

  • For external use only.
  • Flammable, keep away from fire or flame

When Using This Product

  • avoid contact with eyes.
  • if contact occurs, rinse with water.

Stop Using And Ask A Doctor

  • if irritation or redness develops and lasts.

Keep Out Of Reach Of Children.

  • In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

  • apply a small amount in your palm and rub hands together briskly until dry. Children under 6 should be supervised when using this product.

Other Information

do not store above 110°F (43°C)

Questions/Comments?

1-866-322-2439

Inactive Ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Actate, Carbomer, Aminomethyl Propanol, Fragrance (Parfum).

Label Copy

Image Of The Label (17088l)

Image Of The Label (17088l)

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