Hand Sanitizer Gel
FDA Label NDC 50332-0040

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Hart Health for the product Hand Sanitizer (NDC 50332-0040). 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 ingredients, purpose, uses, warnings, when using this product, stop use and ask a doctor if, 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 Ingredients

Ethyl alcohol 62%

Purpose

Antiseptic handwash

Uses

For hanwashing to decrease bacteria on skin. Recommended for repeated use.

Warnings

For external use only

Flammable, keep away from heat and flame

When Using This Product

  • do not use in the eyes
  • in case of contact, rinse eyes throughly with water

Stop Use And Ask A Doctor If

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep Out Of Reach Of Children

If swallowed get medical help or contact a Poison Control Center right away. 1-800-222-1222

Directions

  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6 years of age; use only with adult supervision

Inactive Ingrediends

acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, fragrance, PEG-60 almond glycerides, propylene glycol, purified water, triisopropanolamine

Package Label.Principal Display Panel

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