FDA.reportPublic FDA data

MOISTURIZING HAND SANITIZER GREEN TEA

Manufacturer
Mirfeel Korea Co., Ltd
Effective date
2020-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:27

Label at a glance#

ProductMOISTURIZING HAND SANITIZER GREEN TEA
Active ingredientAlcohol
Label structure9 sections

Indications and uses

ㆍto decrease bacteria on the skin that could cause disease ㆍrecommended for repeated use

Dosage and administration

ㆍwet hands thoroughly with product and allow to dry without wiping ㆍfor children under 6, use only under adult supervision ㆍnot recommended for infants ㆍdo not consume

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Aqua/Water, Carbomer, Aminomethyl Propanol, Jasminum Officinale (Jasmine) Extract, Prunus Mume Flower Extract, Bellis Perennis (Daisy) Flower Extract, Fragrance, Aloe Barbadensis Extract, Tocopheryl Acetate

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

WARNINGS

WARNINGS SECTION

For external use only: hands

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

Flammable. Keep away from fire or flame
--------------------------------------------------------------------------------------------------------
When using this product

ㆍkeep out of eyes. In case of contact with eyes, flush thoroughly with water.
ㆍavoid contact with broken skin ㆍdo not inhale or ingest
--------------------------------------------------------------------------------------------------------
Stop use and ask a doctor if 

ㆍirritation or redness develops ㆍcondition persists for more than 72 hours

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.

Uses

INDICATIONS & USAGE SECTION

ㆍto decrease bacteria on the skin that could cause disease
ㆍrecommended for repeated use

Directions

DOSAGE & ADMINISTRATION SECTION

ㆍwet hands thoroughly with product and allow to dry without wiping
ㆍfor children under 6, use only under adult supervision
ㆍnot recommended for infants
ㆍdo not consume

Other Information

OTHER SAFETY INFORMATION

ㆍstore below 110℉ (43℃) ㆍmay discolor some fabrics
ㆍharmful to wood finishes and plastics

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of pouchImage of pouch

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75010-080-012022-01-28C16284748780-1d6a99b39-7511-a426-e053-dadaa90af4c2e0e1cb94-0308-439d-bd54-fac7bf3515de

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75010-080-01MOISTURIZING HAND SANITIZER GREEN TEA60 mL in 1 POUCHGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75010-080MOISTURIZING HAND SANITIZER GREEN TEA (ETHYL ALCOHOL) GEL [MIRFEEL KOREA CO., LTD]1Legacy NDC, 1 package rows20200620_e0e1cb94-0308-439d-bd54-fac7bf3515de.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
75010-08075010-080-01

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
AminomethylPropanolLU49E6626QIACT
JASMINUM OFFICINALE FLOWER0Q8K841432IACT
PRUNUS MUME FLOWER2N8872050JIACT
BELLIS PERENNIS FLOWER26I94X9A1KIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
d440944c-3e51-4133-a624-25933b0fbfb5e0e1cb94-0308-439d-bd54-fac7bf3515de2020-06-19WarningsExact identifier
spl id: d440944c-3e51-4133-a624-25933b0fbfb5
spl set id: e0e1cb94-0308-439d-bd54-fac7bf3515de

Reported adverse events (FAERS/openFDA)#

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