FLYLEAF WART REMOVER- salicylic acid 20% liquid

Flyleaf WART REMOVER by

Drug Labeling and Warnings

Flyleaf WART REMOVER by is a Otc medication manufactured, distributed, or labeled by Guangzhou Huixue Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 20%

INACTIVE INGREDIENT

Water, Borneol, Glycerin, Polyethylene Glycol, Bisabolol, Allantoin, Lonicera Japonica (Non-eysuckle) Flower Extract, Sophora Augustifolia Root Extract, Hyaluronic Acid.

PURPOSE

Wart remover

INDICATIONS & USAGE

Uses For the removal of warts, including plantar warts, flat warts, common warts, corns, and calluses.

WARNINGS

For external use only. Flammable Keep away from fire and flame. Keep out of reach of children. Avoid contact with eyes, in case of contact, flush eyes with plenty of cool water. Do not swallow, if swallowed, seek medical attention or contact a Poison Control Center (1-800-222-1222) immediately.

KEEP OUT OF REACH OF CHILDREN

Store af room temperature Avoid excessive heat above 37°C (99°F), Skin discoloration may occur during or after use.

WHEN USING

Wash affected area. Soak the wart in warm water for 5 minutes(optional). Use a cotton swab to apply a sufficient amount to cover each wart. Let it dry. Repeat these steps two to three times daily as needed (until the wart is removed) for up to 12 weeks.

DO NOT USE

On irritated skin or on any area that is infct . If you are allergic to any ingredient in this product. . On moles, birthmarks, warts with hair growing from them, genital warts or warts on the face or mucous membranes. .If you have diabetes or poor blood circulation. .If you are pregnant or breastfeeding unless directed by a healthcare practitioner.

STOP USE

Chest pain, rapid heart beat, faintness, or dizziness occurs sudden, unexplained weight gain occurs,your hands or feet swell.

DOSAGE & ADMINISTRATION

Twice each day,(1ml)each time.15 days supply

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FLYLEAF WART REMOVER 
salicylic acid 20% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87204-166
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	6 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
BISABOLOL (UNII: 24WE03BX2T)
ALLANTOIN (UNII: 344S277G0Z)
BORNEOL (UNII: M89NIB437X)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONIC ACID (UNII: S270N0TRQY)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87204-166-01	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/06/2026	02/13/2027

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	02/06/2026	02/13/2027

Labeler - Guangzhou Huixue Biotechnology Co., Ltd. (418186127)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Huixue Biotechnology Co., Ltd.		418186127	manufacture(87204-166)