Hand Sanitizer
FDA Label NDC 50518-306

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Custom Research Labs Inc for the product Hand Sanitizer (NDC 50518-306). 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, other information, inactive ingredients, 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

ANTIMICROBIAL

Uses

  • FOR HANDWASHING TO DECREASE MICROBIAL CONTAMINATION ON THE SKIN
  • MAY BE REAPPLIED DURING THE DAY AS REQUIRED

Warnings

FOR EXTERNAL USE ONLY. DO NOT DRINK.

FLAMMABLE, KEEP AWAY FROM FIRE AND FLAME.

DO NOT USE IN THE EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER, THEN CONTACT PHYSICIAN.

STOP USE AND ASK A DOCTOR IF IRRITATION AND REDNESS DEVELOP AND PERSISTS FOR MORE THAN 72 HOURS

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

Directions

  • WET HANDS THOROUGHLY WITH PRODUCT
  • BRISKLY RUB HANDS TOGETHER UNTIL DRY
  • SUPERVISE CHILDREN UNDER 6 YEARS IN THE USE OF PRODUCT

Other Information

  • STORE AT 20°C TO 25°C (68°F TO 77°F)
    • MAY DISCOLOR SOME FABRICS

Inactive Ingredients

PURIFIED WATER/AQUA/EAU PURIFIE, GLYCERIN, CELLULOSE

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