Nesura Instant Hand Sanitizer

Manufacturer
CELLAB CO., LTD.
Effective date
2020-04-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:36:34

Label at a glance#

ProductNesura Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Uses: ■instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease

Dosage and administration

Directions: ■ Take an appropriate amount on your hands and rub thoroughly to dry.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Ethyl alcohol 70%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Glycerin, Carbomer, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Parfum, Citric Acid, Potassium Sorbate, Sodium Benzoate

PURPOSE

OTC - PURPOSE SECTION

Purpose: antiseptic

WARNINGS

WARNINGS SECTION

Warnings:

For external use only


Flammable, keep away from fire or flame.


When using this product
■ keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ avoid contact with broken skin ■ do not inhale or ingest

Stop use and consult a doctor if
■ irritation and redness occur ■ condition persists for more than 72 hours

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:

■instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

■ Take an appropriate amount on your hands and rub thoroughly to dry.

Other Information

OTHER SAFETY INFORMATION

Other Information
- read the directions and warnings before use
- avoid freezing and excessive heat above 40 degree C (104 degree F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of containerImage of container

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138802070708891GTIN-13: 8802070708891
EAN-13: 8802070708891
GTIN storage (14 digits): 08802070708891
300 container.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57557-110-012024-08-27C16284748780-11030e365-25cc-111a-e063-dadaa90a10e29f6fc8eb-95cd-4275-a407-b8d04ccb4ff6
57557-110-012024-01-30C16284748780-11030e365-25cc-111a-e063-dadaa90a10e29f6fc8eb-95cd-4275-a407-b8d04ccb4ff6

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
57557-11057557-110-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
20b40ee2-436e-f125-e063-6294a90a197d9f6fc8eb-95cd-4275-a407-b8d04ccb4ff62024-08-27WarningsExact identifier
spl set id: 9f6fc8eb-95cd-4275-a407-b8d04ccb4ff6

Reported adverse events (FAERS/openFDA)#

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