BYT BANGYTONG SALICYLIC ACID PATCH- salicylic acid 1% wart remover patch patch

BYT BANGYTONG Salicylic Acid Patch by

Drug Labeling and Warnings

BYT BANGYTONG Salicylic Acid Patch 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

Salicylic acid 1%

Purpose

Wart Remover

Use

For the removal of common warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface

Warnings

For external use only.

Do not use

On irritated,infected, or reddened skin; on genital warts and warts on the face; on moles, birthmarks, and warts with hair growing from them;on mucous mempranes.

When Using

Ask a doctor before use if you have diabetes poor blood circulation

Stop Use

Ask a doctor before use if you have diabetes poor blood circulation

Ask Doctor

Ask a doctor before use if you have diabetes poor blood circulation

Keep Oot Of Reach Of Children

If swallowed, get medical help or contact a Poison control Center right away.

Directions

wash affected area: may soak wart in warm water for 5 minutes dry area thoroughly,remove bandage strips by peeling backing off If necessary,cut medicated patch to fit wart carefully apply medicated plaster, repeat procedure every 48 hours as needed (until wart is removed) for up to 12 week

Other information

Store between 59° and 86°F(15°and 30°C).

Inactive ingredients

hard paraffin,lanolin,phenol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BYT BANGYTONG SALICYLIC ACID PATCH 
salicylic acid 1% wart remover patch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87382-217
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	1 g  in 100

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)
LANOLIN (UNII: 7EV65EAW6H)
PARAFFIN (UNII: I9O0E3H2ZE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87382-217-01	144 in 1 BOX; Type 0: Not a Combination Product	02/02/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	02/02/2026

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

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