Saniultra Hand Sanitizer
FDA Label NDC 76572-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Relief Films, Inc. for the product Saniultra Hand Sanitizer (NDC 76572-101). 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, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

ETHYL ALCOHOL 70%

Purpose

ANTISEPTIC

Uses

TO HELP REDUCE BACTERIA ON SKIN.

Warnings

FOR EXTERNAL USE ONLY.

FLAMMABLE. KEEP AWAY FROM SOURCES OF HEAT OR FIRE.

WHEN USING THIS PRODUCCT AVOID CONTACT WITH EYES. IF CONTACT OCCURS RINSE THOROUGHLY WITH WATER.

STOP USE AND ASK THE DOCTOR IF IRRITATION OR REDNESS DEVELOPS AND PERSISTS.

Otc - Keep Out Of Reach Of Children

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

Directions

  • PUT ENOUGH HAND SANITIZER IN YOUR PALM TO COVER HANDS AND RUB TOGETHER UNTIL DRY.
  • CHILDREN UNDER 5 YEARS SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

Inactive Ingredients

WATER (AQUA), GLYCERIN, CARBOMER, AMINOMETHYL PROPANOL.

Other Information

  • STORE AT THE TEMPERATURE BELOW 110°F (43°C).
  • MAY DISCOLOR CERTAIN FABRICS OR SURFACES.

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