Hand Sanitizer
FDA Label NDC 37808-225

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Heb for the product Hand Sanitizer (NDC 37808-225). 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, uses and directions, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, other information, package front and back labels, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

ETHYL ALCOHOL 62% (ANTISEPTIC)

Uses And Directions

  • USES: TO HELP REDUCE BACTERIA ON THE SKIN.
  • DIRECTIONS: PUT A SMALL AMOUNT INTO YOUR PALM AND BRISKLY RUB HANDS TOGETHER UNTIL DRY.

Warnings

  • FOR EXTERNAL USE ONLY.IN CASE OF ACCIDENTAL INGESTION, SEEK MEDICAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

When Using This Product

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER. AVOID CONTACT WITH BROKEN SKIN.

Stop Use And Ask A Doctor If

SKIN IRRITATION OR REDNESS DEVELOPS.

Keep Out Of Reach Of Children

FOR CHILDREN UNDER 6, USE ONLY WITH ADULT SUPERVISION. NOT RECOMMENDED FOR USE ON INFANTS.

Other Information

FLAMMABLE. KEEP AWAY FROM HEAT AND FLAME.

Package Front And Back Labels

  • 8OZ FRONT AND BACK LABELS: HCF8OZ.jpg
    8oz Front And Back Labels (Hcf8oz)

    8oz Front And Back Labels (Hcf8oz)

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