Purell Gel
FDA Label NDC 67751-188

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Navajo Manufacturing Company Inc. for the product Purell (NDC 67751-188). 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 drug facts, active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

  • Hand sanitized to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

For external use only.

When Using This Product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor If

irritation or rash appears and lasts

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Put enough product in your palm to cover hands and rub hands together briskly until dry
  • Children under 6 years of age should be supervised when using this product

Other Information

  • Store below 110°F (43°C)
  • May discolor certain fabrics or surfaces

Inactive Ingredients

Water (Aqua), Isopropyl Alcohol, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30, Alkly Acrylate, Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum)

Questions?

1-888-4-PURELL www.PURELL.com

Purell, 1Oz

Label4 (Label4)

Label4 (Label4)

Purell, 2Oz

Label5 (Label5)

Label5 (Label5)

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