Subway Alcohol Sanitizer
FDA Label NDC 78016-103

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 Subway Alcohol Sanitizer (NDC 78016-103). 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 62%

Purpose

ANTISEPTIC

Uses

  • DECREASE BACTERIA ON SKIN THAT COULD CAUSE DISEASE
  • RECOMMENDED FOR REPEATED USE

Warnings

FOR EXTERNAL USE ONLY: HANDS

FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.

WHEN USING THIS PRODUCT

  • KEEP OUT OF EYES
  • IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER
  • AVOID CONTACT WITH BROKEN SKIN
  • DO NOT INHALE OR DIGEST

    • STOP USE AND ASK DOCTOR IF

    • IRRITATION OR REDNESS DEVELOPS
    • CONDITION PERSISTS 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 AND ALLOW TO DRY WITHOUT WIPING
  • NOT FOR CHILDREN UNDER 6, USE ONLY UNDER ADULT SUPERVISION
  • NOT RECOMMENDED FOR INFANTS

Inactive Ingredients

DEIONIZED WATER, CARBOPOL, GLYCERIN, FRAGRANCE

* Please review the disclaimer below.