BEE VENOM TAG WART REMOVER- salicylic acid cream

BEE VENOM TAG WART REMOVER by

Drug Labeling and Warnings

BEE VENOM TAG WART REMOVER by is a Otc medication manufactured, distributed, or labeled by Shenzhen Deshijian Medical Equipment Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 5% Wart remover

INACTIVE INGREDIENT

Water, Sodium Hyaluronate, Beta-Glucan, Arginine, Malic Acid, Mandelic Acid,
Bee Venom, Biosaccharide Gum-1, Butylene Glycol, Xanthan Gum, Parfum,
Propylene Glycol, Glyceryl Caprylate, Carbomer, Caprylhydroxamic Acid

PURPOSE

Eliminate all warts, cornsyQuick shedding and no recurrenceySuitable for all skin type

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact the
Poison Control Center (1-800-222-1222) right away.

DOSAGE & ADMINISTRATION

For the removal of common warts and plantar warts. Common warts have a rough
"cauliflower-like" surface and are easily recognizable. Plantar warts are located only
on the soles of the feet, tender to touch, with an interrupted footprint pattern

INDICATIONS & USAGE

Directions:Wash the affected area.May soak wart in warm water for 5 minutes.Dry area thoroughly.Use a brush to apply a sufficient amount to cover each wart. Let it dry.Repeat this procedure once or twice daily as needed (until wart is removed) for upto 12 weeks.

WARNINGS

For external use only. Flammable. Keep away from fire and flame

STOP USE

On irritated skin or on any area that is infected or reddened. 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.

OTHER SAFETY INFORMATION

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

PRINCIPAL DISPLAY PANEL

85741-002-01

INGREDIENTS AND APPEARANCE

BEE VENOM TAG WART REMOVER 
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85741-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ARGININE (UNII: 94ZLA3W45F)
BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
CARBOMER (UNII: 0A5MM307FC)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
PARFUMIDINE (UNII: A2Q2LHC6MA)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
MALIC ACID (UNII: 817L1N4CKP)
APIS MELLIFERA VENOM (UNII: 76013O881M)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)
1,3-BETA-GLUCAN SYNTHASE COMPONENT FKS1 (UNII: 4FRY3LJG0V)
MANDELIC ACID (UNII: NH496X0UJX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85741-002-01	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/29/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	06/29/2025

Labeler - Shenzhen Deshijian Medical Equipment Co., Ltd (445663410)

Registrant - Shenzhen Deshijian Medical Equipment Co., Ltd (445663410)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Deshijian Medical Equipment Co., Ltd		445663410	label(85741-002) , manufacture(85741-002)