FDA.reportPublic FDA data

Bye Bye Germs OMG Hand Foaming

Manufacturer
JK BEAUTY GROUP, INC. | BEAUTY SKIN.CO.,Ltd.
Effective date
2020-06-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:58

Label at a glance#

ProductBye Bye Germs OMG Hand Foaming
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Pump into hands, wet as needed Lather vigorously for at least 10 seconds Wash hands, rinse thoroughly and dry

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush wwith water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump into hands, wet as needed

Lather vigorously for at least 10 seconds

Wash hands, rinse thoroughly and dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Lauric Acid, Myristic Acid, Disodium Laureth Sulfosuccinate, Potassium Hydroxide, 1,2-Hexanediol, Simmondsia Chinensis (Jojoba) Seed Oil, Citric Acid, Lavandula Angustifolia (Lavender) Extract, Aloe Barbadensis Leaf Extract, Beta-Glucan, Sodium Hyaluronate , Hydroxypropyltrimonium Hyaluronate, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronate, Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Potassium Hyaluronate, Ethylhexylglycerin, Sodium Benzoate, Disodium EDTA, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSN1
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCD1
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73724-004-012022-01-28C16284748780-1d6a99b39-5a21-a426-e053-dadaa90af4c2Bye! Bye! Germs OMG! Hand Foaming Soap

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73724-004-01Bye Bye Germs OMG Hand Foaming300 mL in 1 BOTTLE, PUMPSOAP3001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73724-004BYE BYE GERMS OMG HAND FOAMING (BENZALKONIUM CHLORIDE) SOAP [JK BEAUTY GROUP, INC.]1Legacy NDC, 1 package rows20200610_aa1e4839-a281-4bcf-a98c-a05c2eddf6c2.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73724-00473724-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LAURIC ACID1160N9NU9UIACT
MYRISTIC ACID0I3V7S25AWIACT
DISODIUM LAURETH SULFOSUCCINATED6DH1DTN7EIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
JOJOBA OIL724GKU717MIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP9YT4B71U8PIACT
ALOE VERA LEAFZY81Z83H0XIACT
HYALURONATE SODIUMYSE9PPT4THIACT
SODIUM ACETYLATED HYALURONATEWN66R7GL93IACT
HYALURONIC ACIDS270N0TRQYIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
SODIUM BENZOATEOJ245FE5EUIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
a7b06ec1-41e2-7586-e053-2995a90a29dbaa1e4839-a281-4bcf-a98c-a05c2eddf6c22020-06-09WarningsExact identifier
spl id: a7b06ec1-41e2-7586-e053-2995a90a29db
spl set id: aa1e4839-a281-4bcf-a98c-a05c2eddf6c2

Reported adverse events (FAERS/openFDA)#

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