Dr. Nature Hub

Manufacturer
SHIMIZU CO., LTD. | Korea Miracle People Corporation Co.,Ltd
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:13

Label at a glance#

ProductDr. Nature Hub
Active ingredientAlcohol
Label structure9 sections

Indications and uses

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.

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 70.0%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Carbomer, Glycerin, Triethanolamine, Allantoin, Dexpanthenol, Dipotassium Glycyrrhizate, Lavandula Angustifolia (Lavender) Extract, Panax Ginseng Root Extract, Orange Oil, Limonene, Water

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

WARNINGS

WARNINGS SECTION

Flammable. Keep away from fire and flames.

For external use only.


When using this product • Do not get into eyes. • If contact occurs, rinse eyes thoroughly with water.


Stop use and ask a doctor if if irritation or redness develops

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

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.

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.

Package Label: Dr. Nature Hub (1gal)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

Package Label: Dr. Nature Hub (5L)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

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
76901-020-012022-01-28C16284748780-1d6a99b39-db32-a426-e053-dadaa90af4c2ffb3e9b4-ebbb-4946-9846-90a5b49b7565
76901-020-022022-01-28C16284748780-1d6a99b39-db32-a426-e053-dadaa90af4c2ffb3e9b4-ebbb-4946-9846-90a5b49b7565

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76901-020-01Dr. Nature Hub3.78 L in 1 BOTTLE, PUMPGEL3.781
76901-020-02Dr. Nature Hub5 L in 1 BOTTLE, PUMPGEL51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76901-020DR. NATURE HUB (ALCOHOL) GEL [SHIMIZU CO., LTD.]1Legacy NDC, 2 package rows20200605_ffb3e9b4-ebbb-4946-9846-90a5b49b7565.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76901-02076901-020-01, 76901-020-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
224781ba-93ec-4af8-9118-190f0c143ddbffb3e9b4-ebbb-4946-9846-90a5b49b75652020-06-04WarningsExact identifier
spl id: 224781ba-93ec-4af8-9118-190f0c143ddb
spl set id: ffb3e9b4-ebbb-4946-9846-90a5b49b7565

Reported adverse events (FAERS/openFDA)#

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