Instant Hand Sanitizer
FDA Label NDC 63148-225

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Apollo Health And Beauty Care for the product Instant Hand Sanitizer (NDC 63148-225). 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: APPLY A SMALL AMOUNT IN YOUR PALM AND RUB HANDS TOGETHER BRISKLY UNTIL DRY. CHILDREN UNDER 6 SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

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. AVOID CONTACT WITH BROKEN SKIN.

Stop Use And Ask A Doctor If

  • IRRITATION OR RASH DEVELOPS AND LASTS.

Keep Out Of Reach Of Children

  • IF SWALLOWED , GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

Other Information

DO NOT STORE ABOVE 1100F (430C). MAY DISCOLOR CERTAIN FABRICS OR SURFACES.

Package Front And Back Labels

  • 15OZ FRONT AND BACK LABELS: care15.jpg
    15oz Front And Back Labels (Care15)

    15oz Front And Back Labels (Care15)

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