Purell Advanced Hand Sanitizer E3 Gel
FDA Label NDC 21749-711

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Gojo Industries, Llc for the product Purell Advanced Hand Sanitizer E3 Gel (NDC 21749-711). 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, otc - when using, otc - stop use, otc - 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 70% v/v

Purpose

Antimicrobial

Uses

  • Hand sanitizer to help reduce bacteria on the skin that cause disease

Warnings

Flammable. Keep away from fire or flame.

For external use only

Otc - When Using

When using this productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor ifirritation or rash appears and lasts

Otc - Keep Out Of Reach Of Children

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

Directions

  • Place product on hands
  • Rub until dry

Inactive Ingredients

Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

Package Label.Principal Display Panel

Product Label (6461 Label)

Product Label (6461 Label)

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