PureLogic Foaming Hand Sanitizer Lemon Mint

Manufacturer
Argento sc by sicura inc.
Effective date
2020-08-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:23:31

Label at a glance#

ProductPureLogic Foaming Hand Sanitizer Lemon Mint
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry Children under 6 years of age should be supervised when using this product

Storage and handling

To prevent discoloration, avoid contact with clothing

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Purpose: 

Antibacterial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin that could cause disease

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use on hands only.

When using this product

OTC - WHEN USING SECTION

When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water

Do not ingest or inhale

Avoid contact with broken skin

Stop use and ask a doctor

OTC - STOP USE SECTION

if irrigation and redness develop or if condition persists for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry
  • Children under 6 years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

To prevent discoloration, avoid contact with clothing

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium lauroamphoacetate, Cocamidopropylamine oxide, Cocamidopropyl betaine, Glycerin, Olea europaea (olive) leaf extract, Polyminopropyl biguanide, Citric acid, Disodium EDTA, Benzophenone-3, Methylchloroisothiazolinone, Methylisothiazolinone, Fragrance, Cetylpyridinium chloride, Yellow 5 (CI19140)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN1
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD1
1020365benzalkonium chloride 0.13 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77731-053-012022-01-28C16284748780-1d6a99b39-78b1-a426-e053-dadaa90af4c2AB0028LM foaming

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77731-053-01PureLogic Foaming Hand Sanitizer Lemon Mint500 mL in 1 BOTTLESOLUTION5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77731-053PURELOGIC FOAMING HAND SANITIZER LEMON MINT (BENZALKONIUM CHLORIDE) SOLUTION [ARGENTO SC BY SICURA INC.]1Legacy NDC, 1 package rows20200802_7472b2b7-e16e-4d23-a7d1-bf86f465ff32.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77731-05377731-053-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
abd41285-dae2-14a4-e053-2a95a90af6ea7472b2b7-e16e-4d23-a7d1-bf86f465ff322020-08-01WarningsExact identifier
spl id: abd41285-dae2-14a4-e053-2a95a90af6ea
spl set id: 7472b2b7-e16e-4d23-a7d1-bf86f465ff32

Reported adverse events (FAERS/openFDA)#

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