NURSE SOO 70 Hand Sanitizer

Manufacturer
KB Pacific Co., ltd. | EQMAXON Corp.
Effective date
2020-04-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:53

Label at a glance#

ProductNURSE SOO 70 Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Uses: Disinfection of hands and skin

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: ALCOHOL 70.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Carbomer, Butylene Glycol, Aloe Extract, Triethanolamine, Glycerin, Flavor, Sodium Hyaluronate

PURPOSE

OTC - PURPOSE SECTION

Purpose: SANITIZER

WARNINGS

WARNINGS SECTION

Warnings:

1.Do not use the product on the following areas:
Around the eyes and ears, in the mouth, large body parts and damaged skin(Irritation may occur)

2.If you experience any of the following symptoms, discontinue use of the product immediately and consult a physician or pharmacist.
1) Hypersensitivity symptoms, e.g. rash, erythema, itchiness, and edema
2)Skin irritation symptoms

3.Other precautions
1) For external use only (do not swallow).
2) Avoid contact with eyes. If contact occurs, wash with clean water and consult a doctor or pharmacist.
3)Be careful not to inhale vapors in cases of extended or prolonged use. (Repeating inhaling of large amounts of ethanol vapor may cause irritation of the mucous membranes and headaches).
(Limited to ethanol-containing products)
4) If used repeatedly in the same area, care should be provided as the skin may become rough due to excessive oil removal.
5) Do not use sealed bandages, cast bandages, or packs as they may cause irritation.
6) Do not use this drug on the anal or vagina areas, or with hot packs, as it may cause irritation or chemical burns.
7) Use only for the intended purposes.

4.Precautions for storage
1) Keep away from direct sunlight and do not expose the product to heating devices or flame.
2) Keep out of reach of children and go to the hospital immediately if swallowed.
3) After use, close the lid completely to prevent the product from drying or foreign objects from getting inside the container.
4) Storing the product in a different container may cause accidents or deterioration of quality. Therefore, keep the product in its original container.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and go to the hospital immediately if swallowed.

Uses

INDICATIONS & USAGE SECTION

Uses:
Disinfection of hands and skin

Directions

DOSAGE & ADMINISTRATION SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809115169808GTIN-13: 8809115169808
EAN-13: 8809115169808
GTIN storage (14 digits): 08809115169808
nurse carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74082-010-022022-01-28C16284748780-1d6a99b39-ef29-a426-e053-dadaa90af4c2d44e21d1-9ebb-4968-8f37-bb46b9b4f753

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74082-010-01NURSE SOO 70 Hand Sanitizer500 mL in 1 BOTTLE, PUMPGEL5001
74082-010-02NURSE SOO 70 Hand Sanitizer1 in 1 CARTONGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74082-010NURSE SOO 70 HAND SANITIZER (ALCOHOL) GEL [KB PACIFIC CO., LTD.]1Legacy NDC, 2 package rows20200403_d44e21d1-9ebb-4968-8f37-bb46b9b4f753.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74082-01074082-010-01, 74082-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
59e7c9bc-b28e-4d3b-9e15-9ba1cf3fa7b8d44e21d1-9ebb-4968-8f37-bb46b9b4f7532020-04-03WarningsExact identifier
spl id: 59e7c9bc-b28e-4d3b-9e15-9ba1cf3fa7b8
spl set id: d44e21d1-9ebb-4968-8f37-bb46b9b4f753

Reported adverse events (FAERS/openFDA)#

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