FDA.reportPublic FDA data

TNS MEDIPLUS HAND SANITIZER

Manufacturer
Nature Intro Co., Ltd.
Effective date
2020-06-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:17

Label at a glance#

ProductTNS MEDIPLUS HAND SANITIZER
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

• Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 72% v/v

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, carbomer, aloe extract, green tea extract, sodium hyaluronate, aminomethyl propanol, glycerin, orange oil, polysorbate 20, potassium hydroxide, tocopheryl acetate

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame
--------------------------------------------------------------------------------------------------------
Do not use
• in children less than 2 months of age
• on open skin wounds
--------------------------------------------------------------------------------------------------------
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
--------------------------------------------------------------------------------------------------------
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Use(s)

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

Directions

DOSAGE & ADMINISTRATION SECTION

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

OTHER SAFETY INFORMATION

• Store between 15-30℃ (59-86℉)
• Avoid freezing and excessive heat above 40℃ (104℉)

Package Label: TNS MEDIPLUS HAND SANITIZER 100mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

Package Label: TNS MEDIPLUS HAND SANITIZER 500mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

Package Label: TNS MEDIPLUS HAND SANITIZER 1000mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2277550ethanol 72 % Topical GelPSN1
2277550ethanol 0.72 ML/ML Topical GelSCD1
2277550ethanol 72 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78222-010-012022-01-28C16284748780-1d6a99b39-5a44-a426-e053-dadaa90af4c2613e3f65-0461-42a2-ad6b-e1e83c142d23
78222-010-022022-01-28C16284748780-1d6a99b39-5a44-a426-e053-dadaa90af4c2613e3f65-0461-42a2-ad6b-e1e83c142d23
78222-010-032022-01-28C16284748780-1d6a99b39-5a44-a426-e053-dadaa90af4c2613e3f65-0461-42a2-ad6b-e1e83c142d23

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78222-010-01TNS MEDIPLUS HAND SANITIZER100 mL in 1 BOTTLEGEL1001
78222-010-02TNS MEDIPLUS HAND SANITIZER500 mL in 1 BOTTLE, PUMPGEL5001
78222-010-03TNS MEDIPLUS HAND SANITIZER1000 mL in 1 BOTTLE, PUMPGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78222-010TNS MEDIPLUS HAND SANITIZER (ETHYL ALCOHOL) GEL [NATURE INTRO CO., LTD.]1Legacy NDC, 3 package rows20200612_613e3f65-0461-42a2-ad6b-e1e83c142d23.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78222-01078222-010-01, 78222-010-02, 78222-010-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
Water059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALOEV5VD430YW9IACT
GREEN TEA LEAFW2ZU1RY8B0IACT
HYALURONATE SODIUMYSE9PPT4THIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
GlycerinPDC6A3C0OXIACT
ORANGE OILAKN3KSD11BIACT
polysorbate 207T1F30V5YHIACT
potassium hydroxideWZH3C48M4TIACT
.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
b80631a6-28f9-4759-8f9a-f0e5238f0050613e3f65-0461-42a2-ad6b-e1e83c142d232020-06-12WarningsExact identifier
spl id: b80631a6-28f9-4759-8f9a-f0e5238f0050
spl set id: 613e3f65-0461-42a2-ad6b-e1e83c142d23

Reported adverse events (FAERS/openFDA)#

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