OTC Medication Information: DigiClean E

DIGICLEAN E — chloroxylenol solution
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

Chloroxylenol, 1.0%

Purpose

Antiseptic handwash

Uses

  • for handwashing to decrease bacteria on the skin

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

  • 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

  • Wet hands and apply foam
  • Scrub hands and forearms
  • Rinse thoroughly and dry

Other information

  • For additional information see Safety Data Sheet (SDS)
  • For emergency medical information in USA and Canada, call 1-800-328-0026
  • For emergency medical information worldwide, call 1-651-222-5352 (in the USA)

Inactive ingredients

Inactive ingredients water (aqua), propylene glycol, urea, sorbitol, potassium cocoate, tetrasodium EDTA, SD alcohol 3-C, glycerin, sodium xylenesulfonate, citric acid, fragrance, lauramine oxide, FD&C yellow 5, FD&C blue 1

Questions?

Call 1.800.35.CLEAN (352.5326)

Principal Display Panel

DIN 02242847

ECOLAB

23673

6123673

DigiClean™

E Foam Hand Soap

750 mL (25 US FL OZ)

Active Ingredient: Chloroxylenol, 1.0%

705708/5405/0117

This product may be patented

patentado: www.ecolab.com/patents

Ecolab · 1 Ecolab Place · St. Paul MN 55102 U.S.A.

5105 Tomken Road · Mississauga ON L4W 2X5 Canada

© 2017 Ecolab Inc. · All Rights Reserved

Made in United States

705708/5405/0117

Representative label
(click image for full-size original)
DIGICLEAN E
chloroxylenol solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-308
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL 1.0 mg in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
PROPYLENE GLYCOL
UREA
SORBITOL
POTASSIUM COCOATE
EDETATE SODIUM
ALCOHOL
GLYCERIN
SODIUM XYLENESULFONATE
ANHYDROUS CITRIC ACID
LAURAMINE OXIDE
FD&C YELLOW NO. 5
FD&C BLUE NO. 1
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:47593-308-41 750 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 05/26/1999
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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