Instant Hand Sanitizer
FDA Label NDC 37808-253

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 Instant Hand Sanitizer (NDC 37808-253). 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, 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 65% (ANTISEPTIC)

Uses

TO HELP REDUCE BACTERIA ON THE SKIN

Warnings

  • FOR EXTERNAL USE ONLY.
  • FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.

When Using This Product

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

Stop Use And Ask A Doctor If

SKIN IRRITATION OR REDNESS DEVELOPS.

Keep Out Of Reach Of Children

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

Other Information

STORE AT A TEMPERATURE BELOW 1100F (430C).

Package Front And Back Labels

  • 8 OZ Front and Back Labels: hillcountry8.jpg
    8oz Front And Back Labels (Hillcountry8)

    8oz Front And Back Labels (Hillcountry8)

  • 40 OZ Front and Back Labels:hillcountry40.jpg
    40oz Front And Back Labels (Hillcountry40)

    40oz Front And Back Labels (Hillcountry40)

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