Bye Bye Germs Antibacterial Wipes

Manufacturer
Kangna (Zhejiang) Medical Supplies Co., Ltd. | Kangna (Zhejiang) Medical Supply Co., Ltd.
Effective date
2020-10-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:01

Label at a glance#

ProductBye Bye Germs Antibacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Lift tab and pull out towel to wipe hands thoroughly for 30 seconds. Allow to air dry. Reseal after use to prevent moisture from evaporating. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Antiseptic cleanser, helps decrease bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

Avoid contact with the eyes; in case of contact, flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops and persists

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If injested, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • Lift tab and pull out towel to wipe hands thoroughly for 30 seconds. Allow to air dry.
  • Reseal after use to prevent moisture from evaporating.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Polysorbate 20, Disodium EDTA, Phenoxyethanol, Sodium Hydroxide.

Questions?

OTC - QUESTIONS SECTION

Call 1-800-548-4097

Label copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of the labelimage of the label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75109-002-012022-01-28C16284748780-1d6a99b39-c9f9-a426-e053-dadaa90af4c2Drug Facts
75109-002-022022-01-28C16284748780-1d6a99b39-c9f9-a426-e053-dadaa90af4c2Drug Facts
75109-002-032022-01-28C16284748780-1d6a99b39-c9f9-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75109-002-01Bye Bye Germs Antibacterial Wipes75 in 1 POUCHCLOTH751
75109-002-02Bye Bye Germs Antibacterial Wipes75 in 1 CANISTERCLOTH751
75109-002-03Bye Bye Germs Antibacterial Wipes25 in 1 POUCHCLOTH251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75109-002BYE BYE GERMS ANTIBACTERIAL WIPES (BENZALKONIUM CHLORIDE) CLOTH [KANGNA (ZHEJIANG) MEDICAL SUPPLIES CO., LTD.]1Legacy NDC, 3 package rows20201006_6aa2fc38-c077-4b96-81f1-c6c18db56cbf.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75109-00275109-002-01, 75109-002-02, 75109-002-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
9aacc25e-a50a-40da-b75d-b9570a177abd6aa2fc38-c077-4b96-81f1-c6c18db56cbf2020-10-05WarningsExact identifier
spl id: 9aacc25e-a50a-40da-b75d-b9570a177abd
spl set id: 6aa2fc38-c077-4b96-81f1-c6c18db56cbf

Reported adverse events (FAERS/openFDA)#

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