OTC Medication Information: Clean Force

CLEAN FORCE- benzalkonium chloride liquid
Ecolab Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active Ingredient

Benzalkonium chloride 0.1%

Purpose

Antiseptic handwash

Uses

  • for handwashing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

For external use only

Do not use

  • In eyes

When using this product

  • If in eyes, rinse promptly and thoroughly with water
  • discontinue use if irritation and redness develop

Stop use and ask a doctor if  skin irritation or redness occurs for more than 72 hours

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • wash hands to remove soil
  • dispense palmful
  • spread to cover hands, rub in well
  • air dry, do not rinse or towel dry

Other information

  • for additional information, see Safety Data Sheet (SDS)
  • for emergency medical information in USA, call 1.800.328.0026

Inactive ingredients  water (aqua), isopropoyl alcohol, propylene glycol, FD&C red 40, FD&C blue 1

Questions?  call  1.866.444.7450

Principal display panel and representative label

MONOGRAM CLEAN FORCE

CLEANING DISPOSABLES

FOAM 917669

HAND SANITIZER

Hand Care

8000319

750 mL (25 US FL OZ) H13

Active ingredient

Benzalkonium

chloride 0.1%

771920/5400/0917

This product may be patented:

www.ecolab.com/patents

For questions or comments,

call 1-866-444-7450

Manufactured by Distributed by

Ecolab US Foods

1 Ecolab Place Rosemont IL

St. Paul MN 55102 USA Inc 60018 USA

© 2017 Ecolab USA Inc

All rights reserved

Made in U.S.A.

representative label
(click image for full-size original)
CLEAN FORCE
benzalkonium chloride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-586
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
ISOPROPYL ALCOHOL
PROPYLENE GLYCOL
FD&C RED NO. 40
FD&C BLUE NO. 1
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:47593-586-41 750 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 12/20/2017
Labeler — Ecolab Inc. (006154611)

Revised: 05/2023 Ecolab Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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