Universal Sanitizing Spray Lemon & Mint

Manufacturer
Universal Distribution Center Llc
Effective date
2021-02-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:59

Label at a glance#

ProductUNIVERSAL SANITIZING LEMON AND MINT
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• hand sanitizer to decrease bacteria on 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 8-7 inches away from surface and spray evenly. • Allow to air dry for 5 to 10 minutes. Repeat application as necessary • Supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

• store between 15-30° (59-86°F) • Do not expose to temperatures exceeding 50 C/22F.

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 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 piece or burn even after use.

• Protect from 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, 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 8-7 inches away from surface and spray evenly.

• Allow to air dry for 5 to 10 minutes. Repeat application as 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° (59-86°F)

• Do not expose to temperatures exceeding 50 C/22F.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butane, Propane, Isobutane, Parfum.

SPL UNCLASSIFIED SECTION

Kills 99.9% Germs

2in 1

Odor Eliminating & Kills Germs Quickly

Contains 75% Alcohol

KEEP OUT OF REACH OF CHILDREN.

Quick All Purpose Sanitizer

Eliminates Odor & Deodorizes the Air

Fights the Spread of Germs

Prevents Growth of Mold & Mildew

Sanitizes Hard & Soft Surfaces

Mfd for and Distributed By:

Universal Distribution Center LLC

96 Distribution Boulevard, Edison, NJ 08817

Made in Turkey

www.universaldc.com

www.universalbrandsusa.com

NO CFCs

CONTAINS NO CFCs WHICH DEPLETE THE OZONE LAYER

"U" is a Registered Trademark of Universal Distribution Center LLC.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

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
52000-401-002023-07-28C16284748780-10191ceaa-679e-198a-e063-dbdaa90aec3eUniversal Sanitizing Spray Lemon & Mint

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-401-00UNIVERSAL SANITIZING LEMON AND MINT550 mL in 1 CANAEROSOL, SPRAY5501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52000-401UNIVERSAL SANITIZING LEMON AND MINT (ETHYL ALCOHOL) AEROSOL, SPRAY [UNIVERSAL DISTRIBUTION CENTER LLC]1Legacy NDC, 1 package rows20210211_6d51af55-80a7-4c0c-88af-bfa35d5ea08d.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52000-40152000-401-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
BUTANE6LV4FOR43RIACT
PROPANET75W9911L6IACT
ISOBUTANEBXR49TP611IACT

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
c118f15b-a080-4257-8418-5d889412c6706d51af55-80a7-4c0c-88af-bfa35d5ea08d2021-02-09WarningsExact identifier
spl id: c118f15b-a080-4257-8418-5d889412c670
spl set id: 6d51af55-80a7-4c0c-88af-bfa35d5ea08d

Reported adverse events (FAERS/openFDA)#

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