Medi wiper Hand Sanitizing Wipes

Manufacturer
Timk Inc. | NAICO
Effective date
2024-09-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:39:54

Label at a glance#

ProductMedi wiper Hand Sanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

■ Clean with wipes and let dry ■ Do not flush

Label contents#

Full prescribing information#

Active Ingredient

DESCRIPTION SECTION

Benzalkonium Chloride 0.1%

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Glycerin, Sodium Benzoate, Polysorbate 20, Disodium EDTA, Tocopheryl Acetate, Citric Acid

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

For external use only

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Stop use and ask a doctor if
■ hypersensitivity symptoms such as erythema, itching and dermatitis happen
■ skin irritation happens

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Do not use
■ in combination with soap or antibacterial cleansing agents
■ the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin

------------------------------------------------------------------------------

When using this product
■ avoid using repeatedly in the same area, skin irritation may occur
■ avoid getting into the eyes (if contact occurs, wash well with clean water)
■ if following abnormal symptoms persist, discontinue use: Irritation around the eyes, ears, mucous membranes, including the mouth, skin irritation and rashes

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Keep out of reach of children
■ If swallowed, get medical help or contact a Poison Control Center right away

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

Use

INDICATIONS & USAGE SECTION

■ Instant hand antiseptic to decrease bacteria on the skin

Directions

DOSAGE & ADMINISTRATION SECTION

■ Clean with wipes and let dry
■ Do not flush

Other information

DESCRIPTION SECTION

■ Read the directions and warnings before use
■ Avoid freezing and excessive heat above 40°C (104°F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN1
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD1
1038856benzalkonium chloride 0.1 % Medicated WipesSY1
1038856benzalkonium chloride 0.1 % Topical SwabSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83930-010-02Medi wiper Hand Sanitizing Wipes108 g in 1 CONTAINERLIQUID1081

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83930-010MEDI WIPER HAND SANITIZING WIPES (BENZALKONIUM CHLORIDE) LIQUID [TIMK INC.]11 package rows20241202_22c0b37e-b6cb-daaa-e063-6394a90aba7e.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
83930-01083930-010-02

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
22c0b37e-b6cc-daaa-e063-6394a90aba7e22c0b37e-b6cb-daaa-e063-6394a90aba7e2024-09-22WarningsExact identifier
spl id: 22c0b37e-b6cc-daaa-e063-6394a90aba7e
spl set id: 22c0b37e-b6cb-daaa-e063-6394a90aba7e

Reported adverse events (FAERS/openFDA)#

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