Hand Sanitizer Wipes

Manufacturer
KYNC Design LLC
Effective date
2026-01-23
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:35:05

Label at a glance#

ProductHand Sanitizer Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

To Open Package: Flip open dispensing cap. Locate wipe at center of roll and pull through small openning in lid. For best results dispense wipes at an angle. Wet hands thoroughly with product and allow to dry. When finished, snap lid cap shut to retain moisture. Discard wipe in trash receptacle after use. Do not flush.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (CAS NO: 68424-85-1), 0.125% .

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizing wipes help remove bacteria from hands and kill 99.99% of germs. Removes dirt to help with health and cleanliness.

WARNINGS

WARNINGS SECTION

Use on hands only.

Do not use

OTC - DO NOT USE SECTION

If you are allergic to any of the ingredients.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs.

Do not use in or near the eyes.

OTC - WHEN USING SECTION

If contact occurs rinse with plenty of water. Remove contact lenses, if present and easy to do. Continue rinsing. If eye irritation persists, get medical advice/attention.

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

To Open Package: Flip open dispensing cap. Locate wipe at center of roll and pull through small openning in lid. For best results dispense wipes at an angle. Wet hands thoroughly with product and allow to dry. When finished, snap lid cap shut to retain moisture. Discard wipe in trash receptacle after use. Do not flush.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Ethanol, Decyl Glucoside, Glycerine, Aloe Vera Extract, D-Panthenol, Fragrance (Perfume)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

110 mL NDC: 76557-001-01 110ML110ML

245 mL NDC: 76557-001-01 245ML245ML

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2276303benzalkonium Cl 0.125 % Medicated PadPSN8
2276303benzalkonium chloride 1.25 MG/ML Medicated PadSCD8
2276303benzalkonium chloride 0.125 % Medicated WipeSY8
2276303benzalkonium chloride 0.125 % Topical ClothSY8
2276303benzalkonium chloride 0.125 % Topical SwabSY8

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76557-001-03Hand Sanitizer Wipes35 in 1 CANISTERCLOTH358
76557-001-03Hand Sanitizer Wipes3.14 mg in 1 PATCHCLOTH3.148
76557-001-04Hand Sanitizer Wipes75 in 1 CANISTERCLOTH758
76557-001-04Hand Sanitizer Wipes3.14 mg in 1 PATCHCLOTH3.148
76557-001-05Hand Sanitizer Wipes3.14 mg in 1 PATCHCLOTH3.148
76557-001-05Hand Sanitizer Wipes72 in 1 PACKAGECLOTH728

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
76557-00176557-001-04, 76557-001-03, 76557-001-05

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
Hand Sanitizer WipesJUNIPER CLEANKYNC Design LLCa73134a6-8b71-fb0d-e053-2995a90abc062026-01-23WarningsExact identifier
ndc (package): 76557-001-03
ndc (package): 76557-001-05
ndc (package): 76557-001-04
ndc (product): 76557-001
ndc11 (package): 76557000104
ndc11 (package): 76557000105
ndc11 (package): 76557000103
spl id: 491172e1-3f27-ff40-e063-6294a90a7fc5
spl set id: a73134a6-8b71-fb0d-e053-2995a90abc06

Reported adverse events (FAERS/openFDA)#

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