Meijer Wet wipes antibacterial hand wipes

Manufacturer
Ganzhou Olivee Cosmetic Co., Ltd.
Effective date
2023-11-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:19:31

Label at a glance#

ProductMeijer Wet wipes antibacterial hand wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

 adults and children 2 years and over  apply to hands allow skin to dry without wiping  children under 2 years  ask a doctor before use 

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial Agent

Use

INDICATIONS & USAGE SECTION

decreases bacteria on skin

Warnings

WARNINGS SECTION

 For external use only

Do not use

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients

When using the product

OTC - WHEN USING SECTION

do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation occurs or rash develops and continues for more than 72 hours

Keep out of reach from 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 skin to dry without wiping
 children under 2 years ask a doctor before use 

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Alcohol Denat., Phenoxyethanol, PEG-8 Dimethicone, Caprylyl Glycol, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Potassium Sorbate, Disodium EDTA, Citric Acid, Fragrance (Parfum), Aloe Barbadensis Leaf Extract

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1-800-524-1428

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Package

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56136-64556136-645-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
1f074ac8-afa8-ff4e-e063-6294a90ae7147b233b63-5c43-47ec-b96b-e06b6d00fa8a2024-08-06WarningsExact identifier
spl set id: 7b233b63-5c43-47ec-b96b-e06b6d00fa8a

Reported adverse events (FAERS/openFDA)#

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