FDA.reportPublic FDA data

MISSY KAY PREMIUM HAND SANITIZER

Manufacturer
BLIFE | DongbangCosmetics Co., ltd.
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:08:29

Label at a glance#

ProductMISSY KAY PREMIUM HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Uses: Hand sanitizer to help reduce bacteria on the skin that could cause disease

Dosage and administration

Directions: ■ Place enough product in your palm to thoroughly cover your hands ■ Rub hands together briskly until dry ■ Children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: 62.0%(w/w)

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Carbomer, Triethanolamine, Polyoxyethylene Hydrogenated Castor Oil, Lavandula Angustifolia (Lavender) Oil, Methylparaben, Butylene Glycol, Hexylene Glycol, Strawberry Extract, Sophora Extract, Mulberry Root Extract, Glycyrrhiza Extract, Grapefruit Extract, Green Tea Extract

PURPOSE

OTC - PURPOSE SECTION

Purpose: ANTISEPTIC

WARNINGS

WARNINGS SECTION

Warnings:

■ Flammable. Keep away from fire or flame.
■ For external use only
■ When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
■ Stop use and ask a doctor if irritation or rash appears and lasts
■ 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

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

Uses

INDICATIONS & USAGE SECTION

Uses:

Hand sanitizer to help reduce bacteria on the skin that could cause disease

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

■ Place enough product in your palm to thoroughly cover your hands
■ Rub hands together briskly until dry
■ Children under 6 years of age should be supervised when using this product

Other Information

OTHER SAFETY INFORMATION

Other Information
■ Do not store above 110℉(43℃)
■ May discolor certain fabrics or surfaces

Package Label : MISSY KAY PREMIUM HAND SANITIZER (100mL tube)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of tubeImage of tube

Package Label : MISSY KAY PREMIUM HAND SANITIZER (150mL tube)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of tubeImage of tube

Package Label : MISSY KAY PREMIUM HAND SANITIZER (300mL bottle pump)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75006-020-012022-01-28C16284748780-1d6a99b39-5614-a426-e053-dadaa90af4c2a1ad80f2-b9be-49cf-9d41-a74647bdd1e4
75006-020-022022-01-28C16284748780-1d6a99b39-5614-a426-e053-dadaa90af4c2a1ad80f2-b9be-49cf-9d41-a74647bdd1e4
75006-020-032022-01-28C16284748780-1d6a99b39-5614-a426-e053-dadaa90af4c2a1ad80f2-b9be-49cf-9d41-a74647bdd1e4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75006-020-01MISSY KAY PREMIUM HAND SANITIZER100 mL in 1 TUBEGEL1001
75006-020-02MISSY KAY PREMIUM HAND SANITIZER150 mL in 1 TUBEGEL1501
75006-020-03MISSY KAY PREMIUM HAND SANITIZER300 mL in 1 BOTTLE, PUMPGEL3001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75006-020MISSY KAY PREMIUM HAND SANITIZER (ALCOHOL) GEL [BLIFE]1Legacy NDC, 3 package rows20200429_a1ad80f2-b9be-49cf-9d41-a74647bdd1e4.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75006-02075006-020-01, 75006-020-02, 75006-020-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
Water059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
LAVENDER OILZBP1YXW0H8IACT
MethylparabenA2I8C7HI9TIACT
Butylene Glycol3XUS85K0RAIACT
Hexylene GlycolKEH0A3F75JIACT

Source Document#

Source XML · Source PDF

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
f4d945b9-95e4-44b7-8e51-b4fa39eaaecea1ad80f2-b9be-49cf-9d41-a74647bdd1e42020-04-28WarningsExact identifier
spl id: f4d945b9-95e4-44b7-8e51-b4fa39eaaece
spl set id: a1ad80f2-b9be-49cf-9d41-a74647bdd1e4

Reported adverse events (FAERS/openFDA)#

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