Alcohol Free Foaming Hand Sanitizer Soap
FDA Label NDC 65601-700

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Betco Corporation, Ltd. for the product Alcohol Free Foaming Hand Sanitizer (NDC 65601-700). 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 alcohol free foaming hand sanitizer, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Alcohol Free Foaming Hand Sanitizer

​Active Ingredient

Benzalkonium Chloride 0.13%

Uses

  • Hand sanitizer to remove microorganisms on the skin.
  • Use this product when soap and water are not available.

    • Warnings

    • For external use only.
    • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
    • Discontinue use is irritation or redness develops.
    • If irritation persists for more than 72 hours, consult a physician.
    • KEEP OUT OF REACH OF CHILDREN.
    • If swallowed, get medical help or contact a Poison Control Center right away.

      • Directions

      • ​Read the entire label before using this product.
      • ​Dispense 2 pumps of product onto palm of hand and rub thoroughly over all surfaces of both hands until dry.

        • Inactive Ingredients

        Deionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone,  PEG-3 Cocamide, Fragrance, Methyl Chloro Isothiazolinone, Methyl Isothiazolinone,  D&C Green #5.

        Questions or Comments?Phone: (800) 777-9343

        MDS information:​(800) 891-4965

        Purpose

        Antiseptic

        KEEP OUT OF REACH OF CHILDREN

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