Linstol Refreshing and Cleaning Towelette

Manufacturer
Linstol USA, LLC
Effective date
2022-12-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:52:35

Label at a glance#

ProductLinstol Refreshing and Cleaning Towelette
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

Decreases bacteria on skin

Dosage and administration

Adults and children 2 years and over. Apply to hands Allow to dry without wiping children under 2 years Ask a doctor before use

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Decreases bacteria on skin

Warnings

WARNINGS SECTION

For external use only

SPL UNCLASSIFIED SECTION

Flammable: Keep away from flame or high heat

OTC - WHEN USING SECTION

When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use or ask a doctor if irritation or rash appears and lasts.

OTC - QUESTIONS SECTION

  • You may report side effects to FDA at 1-800-FDA-1088.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years and over.
  • Apply to hands
  • Allow to dry without wiping
  • children under 2 years
  • Ask a doctor before use

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Aloe Vera Leaf, Basil, Calendula Officinalis Flower, Ethylhexylglycerin, Fragrance, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol

SPL UNCLASSIFIED SECTION

Distributed by: Linstol USA, LLC
Naples, FL 34114

PRINCIPAL DISPLAY PANEL - 1 Towelette Packet

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REFRESHING & CLEANSING
Towelette

Contains Benzalkonium

1 Towelette

PRINCIPAL DISPLAY PANEL - 1 Towelette Packet
PRINCIPAL DISPLAY PANEL - 1 Towelette Packet

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2371909benzalkonium chloride 1 % Medicated PadPSN3
2371909benzalkonium chloride 10 MG/ML Medicated PadSCD3
2371909benzalkonium chloride 1 % Medicated PadSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76982-8885-92024-01-30C16284748780-11030e365-601d-111a-e063-dadaa90a10e2Linstol Refreshing & Cleaning Towelette

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76982-8885-9Linstol Refreshing and Cleaning Towelette0.0464 mL in 1 PACKETCLOTH0.04643

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76982-8885LINSTOL REFRESHING AND CLEANING TOWELETTE (BENZALKONIUM CHLORIDE) CLOTH [LINSTOL USA, LLC]3Legacy NDC, 1 package rows20221223_8e5bed8f-8549-4622-a05e-5100c7b78321.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
76982-888576982-8885-9

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
f05925d0-c07c-49c9-e053-2a95a90a6aca8e5bed8f-8549-4622-a05e-5100c7b783212022-12-21WarningsExact identifier
spl id: f05925d0-c07c-49c9-e053-2a95a90a6aca
spl set id: 8e5bed8f-8549-4622-a05e-5100c7b78321

Reported adverse events (FAERS/openFDA)#

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