NWK A-FV

Manufacturer
Nae Woi Korea Ltd
Effective date
2021-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:28

Label at a glance#

ProductNWK A-FV
Active ingredientHORSERADISH
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Cochlearia Armoracia (Horseradish) Root Extract

INACTIVE INGREDIENT SECTION

water

OTC - PURPOSE SECTION

anti-virus

WARNINGS SECTION

■ if following abnormal symptoms persist, discontinue use

Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes

■ Stop immediately and consult a doctor if you experience

1) Hypersensitivity symptoms such as erythema, itching and dermatitis.

2) Skin Irritation

3) Following Instructions when using medication

(1) For external use only (Do not use internally)

(2) Avoid getting into the eyes (if contact occurs, wash well with clean water)

■ Be careful not to inhale or use excessively for a long time (ingesting ethanol repeatedly causes irritation to mucous membranes and headaches or other symptoms may appear. When used repeatedly in the same area, skin irritation may occur.

■ Do not use the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin.

It is not recommended to use this one areas that have been medically treated with a cast or bandage.

■ Do not use in combination with soap or antibacterial cleansing agents.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children.

INDICATIONS & USAGE SECTION

apply where needed

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
HORSERADISH Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82081-0001-12025-01-30C16284748780-12cef2736-8aae-d83d-e063-dadaa90ab31fc70ceadd-da19-a7db-e053-2a95a90a1f36

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82081-0001-1NWK A-FV20000 mL in 1 BOTTLELIQUID200001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82081-0001NWK A-FV (COCHLEARIA ARMORACIA(HORSERADISH) ROOT EXTRACT) LIQUID [NAE WOI KOREA LTD]1Legacy NDC, 1 package rows20210714_c70ceadd-da19-a7db-e053-2a95a90a1f36.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82081-000182081-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
HORSERADISH8DS6G120HJACTIB

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
c70cec0a-24ee-cd7b-e053-2a95a90a57b4c70ceadd-da19-a7db-e053-2a95a90a1f362021-07-13WarningsExact identifier
spl id: c70cec0a-24ee-cd7b-e053-2a95a90a57b4
spl set id: c70ceadd-da19-a7db-e053-2a95a90a1f36

Reported adverse events (FAERS/openFDA)#

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