SCOTT

Manufacturer
Kimberly-Clark
Effective date
2026-04-30
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:55:47

Label at a glance#

ProductSCOTT Antiseptic Foam Skin Cleanser
Active ingredientChloroxylenol
Label structure10 sections

Dosage and administration

Lather in hands with water for at least 30 seconds. Rinse well. Children under the age of 6 should be supervised by an adult when using this product.

Storage and handling

Do not store above 110° F (40° C).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 1.75 % w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could potentially cause disease.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Lather in hands with water for at least 30 seconds. Rinse well. Children under the age of 6 should be supervised by an adult when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Hexylene Glycol, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Disodium EDTA, Sodium Hydroxide, Methylchloroisothiazolinone, Methylisothiazolinone.

Other Information

STORAGE AND HANDLING SECTION

Do not store above 110° F (40° C).

SPL UNCLASSIFIED SECTION

Distributed in the U.S. by Kimberly-Clark Global Sales, LLC, Roswell, GA 30076-2199

PRINCIPAL DISPLAY PANEL - 1.2 L Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

91595

Scott® MD

Antiseptic Foam Skin Cleanser

Chloroxylenol Solution

RINSE OFF

20-14-938-0-00

1.2 L (40.5 fl oz / oz liq.)

PRINCIPAL DISPLAY PANEL - 1.2 L Bottle Label
PRINCIPAL DISPLAY PANEL - 1.2 L Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1053758chloroxylenol 1.75 % Medicated Liquid SoapPSN6
1053758chloroxylenol 17.5 MG/ML Medicated Liquid SoapSCD6
1053758chloroxylenol 1.75 % Medicated Liquid SoapSY6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130036000915952GTIN-13: 0036000915952
EAN-13: 0036000915952
GTIN-12: 036000915952
UPC-A: 036000915952
GTIN storage (14 digits): 00036000915952
scott-01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55118-900-10SCOTT Antiseptic Foam Skin Cleanser1 L in 1 BOTTLESOLUTION16
55118-900-12SCOTT Antiseptic Foam Skin Cleanser1.2 L in 1 BOTTLESOLUTION1.26
55118-900-63SCOTT Antiseptic Foam Skin Cleanser6 in 1 CARTONSOLUTION66
55118-900-65SCOTT Antiseptic Foam Skin Cleanser2 in 1 CARTONSOLUTION26

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55118-90055118-900-10, 55118-900-63, 55118-900-12, 55118-900-65

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SCOTT Antiseptic Foam Skin CleanserCHLOROXYLENOLKimberly-Clarkca761935-7dcc-4caf-b941-60693a97c8a62026-04-30WarningsExact identifier
ndc (package): 55118-900-63
ndc (package): 55118-900-65
ndc (package): 55118-900-10
ndc (package): 55118-900-12
ndc (product): 55118-900
ndc11 (package): 55118090010
ndc11 (package): 55118090012
ndc11 (package): 55118090065
ndc11 (package): 55118090063
spl id: 24b97d90-fcd4-49fc-9a77-c449a9b619c1
spl set id: ca761935-7dcc-4caf-b941-60693a97c8a6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.