Klenlii Hand Sanii Alcohol Sanitizer
FDA Label NDC 78016-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Klenlii Company for the product Klenlii Hand Sanii Alcohol Sanitizer (NDC 78016-101). 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, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

ETHYL ALCOHOL 63%

ISOPROPYL ALCOHOL 7%

Purpose

ANTISEPTIC

Uses

  • DECREASE BACTERIA ON SKIN

Warnings

FOR EXTERNAL USE ONLY: HANDS

FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.

WHEN USING THIS PRODUCT

  • KEEP OUT OF EYES

    • STOP USE AND ASK DOCTOR IF

    • IRRITATION OR REDNESS DEVELOPS

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

  • THOROUGHLY WET HANDS WITH PRODUCT AND ALLOW TO DRY

Inactive Ingredients

DEIONIZED WATER, GLYCERIN

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