NEKVNRO FUNGAL NAIL- tolnaftate 1% fungal nail ointment

Nekvnro FUNGAL NAIL by

Drug Labeling and Warnings

Nekvnro FUNGAL NAIL by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

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

Forexternal use only

Do not use

Do not use on children under 2 years of age unless directed by a doctor

When Using

When using this product avoid contact with eyes.

Stop Use

●lrritation occurs

Ask Doctor

● There is no improvement within 4 weeks.

Keep Oot Of Reach Of Children

In case of accidental ingestion, contact a physician, emergency medical carefacility or Poison Control Centerimmediately for advice.

Directions

●Clean affected areas with soap and warm water and dry thoroughly.● Apply a thin layer of 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 toe.

●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 cuticl earea. lf condition persists longer, consult a doctor. ●This product is not effectiveon the scalp or nails.

●Supervise children in the use of this product.

Other information

Store at controlled room temperature 15°-30℃( 59°-86°F) Protect from freezing If freezing occurs warm to room temperature.

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEKVNRO FUNGAL NAIL 
tolnaftate 1% fungal nail ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-029
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)
SALICYLIC ACID (UNII: O414PZ4LPZ)
GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6)
UREA (UNII: 8W8T17847W)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CETYL ALCOHOL (UNII: 936JST6JCN)
ACETIC ACID (UNII: Q40Q9N063P)
MINERAL OIL (UNII: T5L8T28FGP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-029-01	20 g in 1 TUBE; Type 0: Not a Combination Product	09/11/2024
2	NDC: 84010-029-02	30 g in 1 TUBE; Type 0: Not a Combination Product	09/11/2024
3	NDC: 84010-029-03	42.5 g in 1 TUBE; Type 0: Not a Combination Product	09/11/2024
4	NDC: 84010-029-04	50 g in 1 TUBE; Type 0: Not a Combination Product	09/11/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	09/11/2024

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-029)