FDA.reportPublic FDA data

SCOTT Antimicrobial Foam

Manufacturer
Kimberly-Clark
Effective date
2019-10-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:00:51

Label at a glance#

ProductSCOTT Antimicrobial Foam
Active ingredientBenzalkonium Chloride
Label structure11 sections

Dosage and administration

Apply small amount and lather in hands for at least 30 seconds. Adults: Supervise children when using this product. Do not dilute product. For occasional use as needed.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1% w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic cleanser

Use

INDICATIONS & USAGE SECTION

For personal hand hygiene to help prevent the spread of certain bacteria.

Warnings

WARNINGS SECTION

  • For External Use Only. Do not ingest. If swallowed, get medical help or contact a Poison Control Center immediately.
  • Use with caution in children.
  • Avoid contact with eyes. In contact occurs, flush eyes with water.
  • Discontinue use & consult a health care practitioner if irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

OTC - DO NOT USE SECTION

  • Do not use if you are allergic to any ingredients.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply small amount and lather in hands for at least 30 seconds.

SPL UNCLASSIFIED SECTION

Adults: Supervise children when using this product. Do not dilute product. For occasional use as needed.

Other Information

SPL UNCLASSIFIED SECTION

  • Report serious side effects from this product to 1-877-561-6587

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice Powder, Citric Acid, Coco-Betaine, Glycerin, Panthenol, Sodium Benzoate, Sodium Chloride, Sodium Hydroxide, Tocopheryl Acetate, 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

PRINCIPAL DISPLAY PANEL - 33.8 fl oz Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Scott®
Brand

Antimicrobial Foam Soap

Benzalkonium
Chloride Solution, NF

For Domestic / Personal Care Use

Kills 99.9% of most common germs†

1 Liter
(33.8 fl oz)

DIN: 02458675

†Enterococcus faecalis VRE; MDR,
Enterococcus faecium, Pseudomonas aeruginosa,
Escherichia coli, Staphylococcus epidermidis,
Salmonella typhi, Streptococcus pyogenus,
Listeria monocytogenes, Proteus vulgaris,
Salmonella enterica

20-29-382-0-01

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
1038799benzalkonium chloride 0.1 % Topical FoamPSN3
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD3
1038799benzalkonium chloride 0.1 % Topical FoamSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55118-235-632023-01-30C16284748780-1f386c64a-14fd-0266-e053-dadaa90a7c1aSCOTT ® Antimicrobial Foam Soap

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55118-235-10SCOTT Antimicrobial Foam1000 mL in 1 CARTRIDGESOLUTION10003
55118-235-63SCOTT Antimicrobial Foam3 in 1 CARTONSOLUTION33

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55118-235SCOTT ANTIMICROBIAL FOAM (BENZALKONIUM CHLORIDE) SOLUTION [KIMBERLY-CLARK]3Legacy NDC, 2 package rows20191018_e30e0ce8-4fba-48ed-ac6d-ac4f9145a9c4.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
55118-23555118-235-10, 55118-235-63

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
Coco-Betaine03DH2IZ3FYIACT
GlycerinPDC6A3C0OXIACT
Sodium Chloride451W47IQ8XIACT
Sodium BenzoateOJ245FE5EUIACT
Citric Acid Monohydrate2968PHW8QPIACT
AloeV5VD430YW9IACT
PanthenolWV9CM0O67ZIACT
.Alpha.-Tocopherol Acetate9E8X80D2L0IACT
Sodium Hydroxide55X04QC32IIACT

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
ca7440ce-edbd-43bc-b031-730cd5ed6a2de30e0ce8-4fba-48ed-ac6d-ac4f9145a9c42019-10-16WarningsExact identifier
spl id: ca7440ce-edbd-43bc-b031-730cd5ed6a2d
spl set id: e30e0ce8-4fba-48ed-ac6d-ac4f9145a9c4

Reported adverse events (FAERS/openFDA)#

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