FDA.reportPublic FDA data

Scott Moisturizing Foam Hand Sanitizer (Ultra)

Manufacturer
Kimberly-Clark
Effective date
2019-10-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:01:00

Label at a glance#

ProductScott Moisturizing Foam Hand Sanitizer (Ultra)
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Use enough foam to cover your hands. Rub hands together briskly until 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

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Flammable - Keep away from open flame and sources of heat.

For External Use Only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes; in case of contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use & ask a health care practitioner 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 Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Use enough foam to cover your hands. Rub hands together briskly until 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).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Betaine, Camellia Sinensis Leaf Extract, Citric Acid, Cucumis Sativus (Cucumber) Fruit Extract, Glycerin, Isopropanol, Meadowfoamamidopropyl Betaine, Panthenol, PEG-10 Dimethicone, Water/Eau

Questions?

OTC - QUESTIONS SECTION

1-888-346-4652

SPL UNCLASSIFIED SECTION

Distributed in the U.S. by Kimberly-Clark Global Sales, LLC,
Roswell, GA 30076-2199. Distributed in Canada by Kimberly-Clark Inc.,
Mississauga, Ontario L5B 3Y5.

PRINCIPAL DISPLAY PANEL - 33.8 fl oz Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

34700

SAME GREAT
FORMULATION.
Now Scott®
branded!

Scott®
Brand

Moisturizing
Foam Hand Sanitizer

ULTRA
Leave On

Empty &
Discard Pump
PLASTIC
BOTTLE

20-14-658-0-03

how2recycle.info

ECOLOGO
PRODUCT CERTIFIED FOR
REDUCED ENVIRONMENTAL
IMPACT. VIEW SPECIFIC
ATTRIBUTES EVAUATED:
UL.COM/EL UL 2783

NPN: 80030706

For Personal / Domestic Use Only

1 Liter (33.8 fl oz)

Principal Display Panel - 33.8 fl oz Bottle Label
Principal Display Panel - 33.8 fl oz Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN2
616805ethanol 0.7 ML/ML Topical FoamSCD2
616805ethanol 70 % 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
55118-532-632023-01-30C16284748780-1f386c649-d36d-0266-e053-dadaa90a7c1aScott ® Moisturizing Foam Hand Sanitizer (Ultra)
55118-532-652023-01-30C16284748780-1f386c649-d36d-0266-e053-dadaa90a7c1aScott ® Moisturizing Foam Hand Sanitizer (Ultra)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55118-532-10Scott Moisturizing Foam Hand Sanitizer (Ultra)1000 mL in 1 BOTTLESOLUTION10002
55118-532-12Scott Moisturizing Foam Hand Sanitizer (Ultra)1200 mL in 1 BOTTLESOLUTION12002
55118-532-63Scott Moisturizing Foam Hand Sanitizer (Ultra)6 in 1 CARTONSOLUTION62
55118-532-65Scott Moisturizing Foam Hand Sanitizer (Ultra)2 in 1 CARTONSOLUTION22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55118-532SCOTT MOISTURIZING FOAM HAND SANITIZER (ULTRA) (ALCOHOL) SOLUTION [KIMBERLY-CLARK]2Legacy NDC, 4 package rows20191019_6658934b-a1f0-4931-a528-15cee3a91fa7.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55118-53255118-532-10, 55118-532-63, 55118-532-12, 55118-532-65

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
Betaine3SCV180C9WIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
CUCUMBERYY7C30VXJTIACT
GlycerinPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
MEADOWFOAMAMIDOPROPYL BETAINEHNV0L650LGIACT
PanthenolWV9CM0O67ZIACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
Water059QF0KO0RIACT

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
c9712f1c-bcd6-4e39-a19a-82bfffcd47216658934b-a1f0-4931-a528-15cee3a91fa72019-10-18WarningsExact identifier
spl id: c9712f1c-bcd6-4e39-a19a-82bfffcd4721
spl set id: 6658934b-a1f0-4931-a528-15cee3a91fa7

Reported adverse events (FAERS/openFDA)#

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