FRESH PURE HAND

Manufacturer
Ester Co., Ltd.
Effective date
2020-11-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:33:40

Label at a glance#

ProductFRESH PURE HAND
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Uses: For handwashing when water is not available to decrease bacteria on the skin - After changing diapers -  After assisting ill persons -  Before contact with a person under medical care or treatment -  Recommended for repeated use

Dosage and administration

Directions: -  Apply palmful to hands -  Rub hands together vigorously until dry -  Supervise children in the use of this product

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: ALCOHOL 70%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Butylene Glycol, Carbomer, Triethanolamine, Polysorbate 60, Isopropyl Myristate, Fragrance

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 redness develops.

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

Uses

INDICATIONS & USAGE SECTION

Uses:

For handwashing when water is not available to decrease bacteria on the skin
- After changing diapers
-  After assisting ill persons
-  Before contact with a person under medical care or treatment
-  Recommended for repeated use

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

-  Apply palmful to hands
-  Rub hands together vigorously until dry
-  Supervise children in the use of this product

Other Information

OTHER SAFETY INFORMATION

Other Information:
Store at room temperature: 15°~30 °C (59°~86 °F)

PACKAGE LABEL - FRESH PURE HAND GEL 30mL * 20ea Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

PACKAGE LABEL - FRESH PURE HAND GEL 500mL Bottle

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74004-030-022022-01-28C16284748780-1d6a99b39-e69a-a426-e053-dadaa90af4c2c56c0300-ef45-4d54-968e-74d0ba1fec64
74004-030-032022-01-28C16284748780-1d6a99b39-e69a-a426-e053-dadaa90af4c2c56c0300-ef45-4d54-968e-74d0ba1fec64

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74004-030-01FRESH PURE HAND30 mL in 1 POUCHGEL302
74004-030-02FRESH PURE HAND20 in 1 CARTONGEL202
74004-030-03FRESH PURE HAND500 mL in 1 BOTTLE, PUMPGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74004-030FRESH PURE HAND (ALCOHOL) GEL [ESTER CO., LTD.]2Legacy NDC, 3 package rows20201114_c56c0300-ef45-4d54-968e-74d0ba1fec64.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74004-03074004-030-01, 74004-030-02, 74004-030-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
b3e0bc1d-2112-c005-e053-2a95a90a89d6c56c0300-ef45-4d54-968e-74d0ba1fec642020-11-11WarningsExact identifier
spl id: b3e0bc1d-2112-c005-e053-2a95a90a89d6
spl set id: c56c0300-ef45-4d54-968e-74d0ba1fec64

Reported adverse events (FAERS/openFDA)#

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