Tork Premium Hand Sanitizer Foam
FDA Label NDC 49351-018

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sca Tissue North America for the product Tork Premium Hand Sanitizer Foam (NDC 49351-018). 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, use, warnings, directions, inactive ingredients, principal display panel - 800ml carton, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 67% v/v

Purpose

Antiseptic cleanser

Use

  • To decrease potentially harmful germs on skin.

Warnings

  • Flammable. Keep away from fire or flame
  • For external use only.

Directions

  • Apply generously to hands.
  • Rub hands together.
  • Allow hands to dry.
  • Repeat daily as necessary.

Inactive Ingredients

Water (Aqua), DEA-C8-18 Perfluoroalkylethyl Phosphate, Aloe Vera, Glycerin

Principal Display Panel - 800Ml Carton

TORK®
Premium
40 02 14A

Hand Sanitizer
Foam
with 67% Ethyl Alcohol

S21 System

27 fl oz
800ml

SCA

Principal Display Panel (800ml Carton)

Principal Display Panel (800ml Carton)

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