UltraClean

Manufacturer
SIRIUS ENDUSTRI YATIRIMLARI VE PLASTIK SANAYI ANONIM SIRKETI
Effective date
2020-06-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:30

Label at a glance#

ProductUltraClean
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

Wet hands thoroughly with the product and allow it to dry, discard after use. Children under 6 years of age should be supervised when using UltraClean Products.

Storage and handling

Avoid excessive heat or freezing. Store between 15-30 C. Dispose the used wipe in trash, do not flush it into the toilet. The product may discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.115%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For sanitizing to help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Not edible, don't drink. Do not use in ears or mouth.

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Wet hands thoroughly with the product and allow it to dry, discard after use.

Children under 6 years of age should be supervised when using UltraClean Products.

Other information

STORAGE AND HANDLING SECTION

  • Avoid excessive heat or freezing. Store between 15-30 C.
  • Dispose the used wipe in trash, do not flush it into the toilet.
  • The product may discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, citric acid, lime oil, Cocamidopropyl betaine, Phenoxyethanol, Polysorbate 20, peg-7 glyceryl cocoate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

72 PCS NDC: 77222-224-0172 PCS NDC: 77222-224-0172 PCS NDC: 77222-224-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049374benzalkonium Cl 0.115 % Medicated PadPSN1
1049374benzalkonium chloride 1.15 MG/ML Medicated PadSCD1
1049374benzalkonium chloride 0.115 % Medicated PadSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77222-224-012021-07-23C16284748780-1c7ccaba7-2673-fd44-e053-dadaa90aa01bSIRIUS-UltrClean Wet Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77222-224-01UltraClean72 in 1 PACKAGESWAB721
77222-224-01UltraClean100 mL in 1 NOT APPLICABLESWAB1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77222-224ULTRACLEAN (SANITIZER WET WIPES) SWAB [SIRIUS ENDUSTRI YATIRIMLARI VE PLASTIK SANAYI ANONIM SIRKETI]1Legacy NDC, 2 package rows20200622_a8814e54-0e51-87bd-e053-2a95a90a30a7.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77222-22477222-224-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
a8813aaa-8e61-352c-e053-2a95a90a783fa8814e54-0e51-87bd-e053-2a95a90a30a72020-06-20WarningsExact identifier
spl id: a8813aaa-8e61-352c-e053-2a95a90a783f
spl set id: a8814e54-0e51-87bd-e053-2a95a90a30a7

Reported adverse events (FAERS/openFDA)#

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