BYT BANGYTONG HELPS WITH NAGELPILZ- tolnaftate 1% helps with nagelpilz liquid liquid

BYT BANGYTONG HELPS WITH NAGELPILZ by

Drug Labeling and Warnings

BYT BANGYTONG HELPS WITH NAGELPILZ by is a Otc medication manufactured, distributed, or labeled by Shenzhen Jindali Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Tolnaftate 1%

Purpose

Antifungal

Use

Antifungal treatment for fingernails,toenails, and surrounding skin.Effective against fungal nails and athlete's foot caused by fungi.

Warnings

For external use only.

Do not use

if you experience any signs of sensitivity or irritation

When Using

Not for use in the eyes, mouth,or vaginal area.

Stop Use

If the area of application shows increased irritation

If there is Consult a doctor if symptoms worsen.

If pregnant or breastfeeding

Ask Doctor

If the area of application shows increased irritation
If there is Consult a doctor if symptoms worsen.
If pregnant or breastfeeding

Keep Oot Of Reach Of Children

If accidental ingestion occurs,seek medical assistance or contact a Poison Control Center immediately.

Directions

For athlete's foot and ringworm：use daily for 4 weeks.Clean the affected area and dry thoroughly.Keep away from fire and flames.For external use on nails and the immediately adjacent skin only.Use once daily, preferably before bedtime.

Unscrew the bottle cap and use the brush to apply the medicine directly to the nail.The medication will then penetrate deeply into the nail.If the nail area is infected,spray the medication onto the affected area.
SHAKE WELL BEFORE USE.
Store at 5°C to 30°C(41°F to 86°F) in a cool dry place.
Keep tightly closed and away from sunlight.

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BYT BANGYTONG HELPS WITH NAGELPILZ 
tolnaftate 1% helps with nagelpilz liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87382-097
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
PSEUDOLARIX AMABILIS BARK (UNII: 49G13A93VE)
WATER (UNII: 059QF0KO0R)
EUPHORBIA HIRTA WHOLE (UNII: L13YF113GN)
HYDRACRYLIC ACID (UNII: C4ZF6XLD2X)
RESORCINOL (UNII: YUL4LO94HK)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87382-097-02	3 in 1 BOX	03/06/2026
1		2.5 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 87382-097-01	2.5 mL in 1 TUBE; Type 0: Not a Combination Product	03/06/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	03/06/2026

Labeler - Shenzhen Jindali Technology Co., Ltd (722786197)

Registrant - Shenzhen Jindali Technology Co., Ltd (722786197)