NAIL FUNGUS TREATMENT- tolnaftate 1% nail fungus treatment liquid

NAIL FUNGUS TREATMENT by

Drug Labeling and Warnings

NAIL FUNGUS TREATMENT by is a Otc medication manufactured, distributed, or labeled by Shenzhen Bullfighting Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Tolnaftate 1%

Purpose

Antifungal

Use

For the effective treatment of nailfungus, discoloration, thickening,splitting, crumbling, and brittleness.

Warnings

Avoid contact with eyes, mouth, andopen wounds. Rinse immediately ifexposed.If irritation persists, seekmedical help.keep out of reach ofchildren and pets.

Do not use

On damaged skin (cuts, abrasions,eczema, sunburn).

lfyou have diabetes or poor bloodcirculation.

When Using

Skin discoloration may occur during or after use.

Stop Use

If irritation occurs. If an allergic reaction occurs.

Ask Doctor

if you are pregnant or breastfeeding.
if you have diabetes.

Keep Out Of Reach Of Children

Keep out of reach of children and pets.

If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1222).
Children should use under adult supervision.

Directions

Soak the affected nail inwarm water to soften it. Gently file thenail to thin it and remove dirt, beingcautious not to harm the nail bed.
Application: Apply full layers of thesolution with the brush onto affectedareas on, around, and under the nails.A light tingle or burn is normal for thefirst 10 minutes until absorbed.
Frequency: Use twice daily (morningand night). Visible results may appearin 6 weeks. Continue regular use toprevent regrowth.

Other information

Store between 15°C to 30'C(59'F to86°F). Avoid freezing and excessiveheat above 40°C (104°F).

Inactive ingredients

Euphorbia hirta whole, Glycerin, Hydracrylic Acid, Pseudolarix amabilis bark, Resorcinol, Water

Questions

Email: douniu1@outlook.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NAIL FUNGUS TREATMENT 
tolnaftate 1% nail fungus treatment liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85834-001
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)
PSEUDOLARIX AMABILIS BARK (UNII: 49G13A93VE)
RESORCINOL (UNII: YUL4LO94HK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85834-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/30/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	06/30/2025

Labeler - Shenzhen Bullfighting Trading Co., Ltd. (614604553)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Bullfighting Trading Co., Ltd.		614604553	manufacture(85834-001)