Sanitol London Sanitizing SPRAY

Manufacturer
Endeks Kimya Sanayi Ve Ticaret Anonim Sirketi
Effective date
2020-09-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:28:37

Label at a glance#

ProductSanitol London Sanitizing
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available

Dosage and administration

• Shake well before use. • Hold can upright at 6-7 inches away from surface and spray evenly. • Allow to air dry for 5 to 10 minutes. Repeat application a necessary • Supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

• store between 15-30°C (59-86°F) • Do not expose to temperatures exceeding 50 C/122 F.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer to decrease bacteria on the skin

• recommended for repeated use

• for use when soap and water are not available

Warnings

WARNINGS SECTION

• Extremely flammable aerosol, keep away from fire / flame.

• Keep away from heat, hot surfaces, open flames and other ignition sources.

• Pressurized container. Do not pierce or burn even after use.

• Protect from the sunlight.

• For external use only.

Do not use

• on children less than 2 months of age

• on open skin wounds

When using this product • Avoid use on/or around eyes, ears, mouth, broken/irritated skin or large

areas of body. In case of contact with eyes, rinse thoroughly with water several minutes. • do not

inhale or ingest.

Stop and ask doctor if

• irritation persist

• or if product is swallowed

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

• Shake well before use.

• Hold can upright at 6-7 inches away from surface and spray evenly.

• Allow to air dry for 5 to 10 minutes. Repeat application a necessary

• Supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

• store between 15-30°C (59-86°F)

• Do not expose to temperatures exceeding 50 C/122 F.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butane, Propane, Isobutane, Parfum, Glycerin

SPL UNCLASSIFIED SECTION

KILLS 99.9%  OF VIRUSES BACTERIA

ELIMINATES ODORS

ALCOHOL CONTENT 75 %

Rinse Free Protection

FRESH LINEN

Sanitizer Spray

*Effective at eliminating 99.9% of many common harmful germs and bacteria in as little as 15 seconds

You may also report any serious side effects to PO Box 328, Wood Ridge, NJ 07075-328

packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitleduntitled

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN1
2286295ethanol 0.75 ML/ML Topical SpraySCD1
2286295ethanol 75 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78089-042-012022-01-28C16284748780-1d6a99b39-afa2-a426-e053-dadaa90af4c2Sanitol London Sanitizing SPRAY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78089-042-01Sanitol LondonSanitizing600 mL in 1 BOTTLE, SPRAYAEROSOL, SPRAY6001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78089-042SANITOL LONDON SANITIZING (ETHYL ALCOHOL) AEROSOL, SPRAY [ENDEKS KIMYA SANAYI VE TICARET ANONIM SIRKETI]1Legacy NDC, 1 package rows20200908_7bd0c7e6-70cd-41a9-beee-81a8a1ddb987.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
78089-04278089-042-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
11e3e50f-403c-4920-8cf4-d099a08982da7bd0c7e6-70cd-41a9-beee-81a8a1ddb9872020-09-04WarningsExact identifier
spl id: 11e3e50f-403c-4920-8cf4-d099a08982da
spl set id: 7bd0c7e6-70cd-41a9-beee-81a8a1ddb987

Reported adverse events (FAERS/openFDA)#

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