Anti-bacterial Hand Sanitizer
FDA Label NDC 77027-112

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Zuofun Cosmetics Co., Ltd. for the product Anti-bacterial Hand Sanitizer (NDC 77027-112). 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 ingredients, purpose, uses, warnings, 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 Ingredients

ETHYL ALCOHOL 75%

Purpose

Antiseptic

Uses

  • FOR HANDWASHING TO DECREASE BACTERIA ON THE HAND

Warnings

  • FOR EXTERNAL USE ONLY. FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME
  • DO NOT USE IN THE EYES

    • STOP USE AND ASK A DOCTOR IF:

    • IRRITATION AND REDNESS DEVELOP
    • CONDITION PERSISTS FOR MORE THAN 72 HOURS

Keep Out Of Reach Of Children.

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

Directions

WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOUT WIPING.

Other Information

CUSTOMER SUPPORT OR TO REPORT A SERIOUS ADVERSE EVENT, CONTACT 1-888-986-3861

Inactive Ingredients

AQUA, PROPYLENE GLYCOL, GLYCEROL, CARBOMER, AMINOMETHYL PROPANOL

Product Image

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