SCOTT Moisturizing Foam Hand Sanitizer

Manufacturer
Kimberly-Clark Corporation
Effective date
2021-07-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:41:39

Label at a glance#

ProductSCOTT Moisturizing Foam Hand Sanitizer
Active ingredientAlcohol
Label structure11 sections

Indications and uses

For personal hand hygiene to help prevent the spread of bacteria. Kills harmful bacteria or germs.

Dosage and administration

Use enough foam to cover your hands. Supervise children when they use this product. For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. Use as part of your daily cleansing routine.

Storage and handling

Report serious side effects from this product to 1-877-561-6587. Do not store above 110 °F (40 °C).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Product Facts

Medicinal ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic cleanser

Uses

INDICATIONS & USAGE SECTION

For personal hand hygiene to help prevent the spread of bacteria. Kills harmful bacteria or germs.

Warnings

WARNINGS SECTION

For external use only

Flammability warning

SPL UNCLASSIFIED SECTION

Keep away from open flame and sources of heat.

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 or persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a poison control centre right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Use enough foam to cover your hands. Supervise children when they use this product. For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. Use as part of your daily cleansing routine.

Other information

STORAGE AND HANDLING SECTION

Report serious side effects from this product to 1-877-561-6587. Do not store above 110 °F (40 °C).

Non-medicinal ingredients

INACTIVE INGREDIENT SECTION

Betaine, Fragrance/Parfum, Meadowfoam Amidopropyl Betaine, PEG-10 Dimethicone, PEG-7 Gylceryl Cocoate, Water/Eau/Aqua

Questions?

OTC - QUESTIONS SECTION

1-888-346-4652

SPL UNCLASSIFIED SECTION

Imported and distributed in Canada by Kimberly-Clark Inc.,
Mississauga, Ontario L5B 3Y5.

PRINCIPAL DISPLAY PANEL - 1.2 Liter Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Scott®
Brand

SAME GREAT
FORMULATION.
Now Scott®
branded!

Moisturizing Foam Hand Sanitizer

Hydrates skin

LEAVE ON

1.2 Liters (40.5 fl oz)

Principal Display Panel - 1.2 Liter Bottle Label
Principal Display Panel - 1.2 Liter Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616763ethanol 62 % Topical FoamPSN2
616763ethanol 0.62 ML/ML Topical FoamSCD2
616763ethanol 62 % Topical FoamSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55118-703-122023-01-30C16284748780-1c7ccaba7-23c4-fd44-e053-dadaa90aa01bSCOTT ® Moisturizing Foam Hand Sanitizer
55118-703-122021-07-23C16284748780-1c7ccaba7-23c4-fd44-e053-dadaa90aa01bSCOTT ® Moisturizing Foam Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55118-703-12SCOTT Moisturizing Foam Hand Sanitizer1200 mL in 1 BOTTLE, PUMPSOLUTION12002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55118-703SCOTT MOISTURIZING FOAM HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]2Legacy NDC, 1 package rows20210724_d481c4bb-78a8-4941-a712-18881f7f0610.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55118-70355118-703-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

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
c01ecab6-8a28-4431-8f35-82ca54eb62d2d481c4bb-78a8-4941-a712-18881f7f06102021-07-22WarningsExact identifier
spl id: c01ecab6-8a28-4431-8f35-82ca54eb62d2
spl set id: d481c4bb-78a8-4941-a712-18881f7f0610

Reported adverse events (FAERS/openFDA)#

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