NWK A-FV (cochlearia armoracia- horseradish root extract liquid

NWK A-FV by

Drug Labeling and Warnings

NWK A-FV by is a Otc medication manufactured, distributed, or labeled by Nae Woi Korea Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Cochlearia Armoracia (Horseradish) Root Extract

INACTIVE INGREDIENT

water

PURPOSE

anti-virus

WARNINGS

■ 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.

KEEP OUT OF REACH OF CHILDREN

Keep Out of Reach of Children.

INDICATIONS & USAGE

apply where needed

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NWK A-FV 
cochlearia armoracia(horseradish) root extract liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82081-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HORSERADISH (UNII: 8DS6G120HJ) (HORSERADISH - UNII:8DS6G120HJ)	HORSERADISH	10 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82081-0001-1	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/14/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/14/2021

Labeler - Nae Woi Korea Ltd (689702988)

Registrant - Nae Woi Korea Ltd (689702988)

Establishment
Name	Address	ID/FEI	Business Operations
Nae Woi Korea Ltd		689702988	manufacture(82081-0001)