NEKVNRO FUNGAL NAIL TREATMENT KIT FUNGAL NAIL OINTMENT.- fungal nail treatment kit fungal nail ointment. paste NEKVNRO FUNGAL NAIL TREATMENT KIT MULTI-PURPOSE TREATMENT.- fungal nail treatment kit multi-purpose treatment. liquid

Nekvnro Fungal Nail Treatment Kit Multi-Purpose Treatment. by

Drug Labeling and Warnings

Nekvnro Fungal Nail Treatment Kit Multi-Purpose Treatment. by is a Otc medication manufactured, distributed, or labeled by Guoyu Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

30G:

Tolnaftate 1%

50ML:

Tolnaftate 1%

Purpose

Anti-fungal

Use

■Proven effective in the treatment of most athlete’s foot (tinea pedis) and ringworm(tinea corporis).
■Helps prevent most athlete's foot with daily use.

■For effective relief of itching, burning and cracking.

Warnings

For external use only.

Do not use

on children under 2 years of age unless directed by a doctor.

When Using

this product avoid contact with eyes.

Stop Use

and ask a doctor if
■Irritation occurs.

■There is no improvement within 4 weeks.

Ask Doctor

■Irritation occurs.

■There is no improvement within 4 weeks.

Keep Oot Of Reach Of Children

In case of accidental ingestion, contact a physician, emergency medical care facility or Poison Control Center immediately for advice.

Directions

■Clean affected areas with soap and warm water and dry thoroughly.

■Apply a thin layer of Nekvnro Anti-Fungal Ointment over affected area twice daily (morning and night) or as directed by a doctor.

■ Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.

■ For athlete’s foot pay special attention to spaces between the toes.

■For athlete’s foot and ringworm, use daily for 4 weeks.

■To prevent athlete's foot, apply once or twice daily(morning and/or night).

■For toe fungus, apply under nail and around cuticle area.If condition persists longer, consult a doctor.

■ This product is not effective on the scalp or nails.

■Supervise children in the use of this product.

Other information

Store at controlled room temperature 15º-30º C( 59º-86ºF) Protect from freezing.If freezing occurs warm to room temperature.

Inactive ingredients

30G:

Cetyl alcohol, Glycerin, Monoolein, Salicylic acid,Stearyl alcohol, Urea, Acetic acid，mineral oil，etc.

30ML:

water, euphorbia hirta whole, glycerin, hydracrylic acid, pseudolarix amabilis bark, resorcinol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEKVNRO FUNGAL NAIL TREATMENT KIT FUNGAL NAIL OINTMENT. 
fungal nail treatment kit fungal nail ointment. paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84844-016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
ACETIC ACID (UNII: Q40Q9N063P)
MINERAL OIL (UNII: T5L8T28FGP)
UREA (UNII: 8W8T17847W)
CETYL ALCOHOL (UNII: 936JST6JCN)
SALICYLIC ACID (UNII: O414PZ4LPZ)
GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84844-016-01	30 g in 1 TUBE; Type 0: Not a Combination Product	11/21/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	11/21/2024

NEKVNRO FUNGAL NAIL TREATMENT KIT MULTI-PURPOSE TREATMENT. 
fungal nail treatment kit multi-purpose treatment. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84844-017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
EUPHORBIA HIRTA WHOLE (UNII: L13YF113GN)
HYDRACRYLIC ACID (UNII: C4ZF6XLD2X)
WATER (UNII: 059QF0KO0R)
PSEUDOLARIX AMABILIS BARK (UNII: 49G13A93VE)
RESORCINOL (UNII: YUL4LO94HK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84844-017-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/21/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	11/21/2024

Labeler - Guoyu Trading Co., Ltd. (963348600)

Establishment
Name	Address	ID/FEI	Business Operations
Guoyu Trading Co., Ltd.		963348600	manufacture(84844-016, 84844-017)