TAG WART REMOVER- salicylic acid 10% liquid

Tag wart remover by

Drug Labeling and Warnings

Tag wart remover by is a Otc medication manufactured, distributed, or labeled by Hengyang Chuangjiujia Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

salicylic acid 10%

PURPOSE

Removing warts

INDICATIONS & USAGE

For the removal of genital, plantarcommon, and fat warts
the common wart is easily recognizedbythe rough cauliflower-like appearanceotthe surface
the plantar wart is recognized byitslocation only on the bottom of thefoot, itstenderness and the interruptionof thefootprint pattern

WARNINGS

For external use only
Keep away from fire and flame
Do not touch by children

WHEN USING

avoid contact with eyes. lf the productgetsinto the eye, flush with water for 15minutes
eavoid inhaling vapors
cap the tube tiahtlv
out of direct sunlight and store atroomtemperature away from heat

STOP USE

if discomfort persists.
if you have diabetes or poor bloodcirculation.

KEEP OUT OF REACH OF CHILDREN

If swallowed, seekimmediate medical attention (1-800-222-1222)

DOSAGE & ADMINISTRATION

wash the affected area
may soak the wart in warm water for 5 minutes
dry area thoroughly
using the applicator(cotton swab),apply alayer of ointment to sufhcientlycovereachwart
allow it to fully absorb and cover it withobandage as needed.
repeat this procedure once or twice dailyasneeded (until the wart is removed) for upto12 weeks

INACTIVE INGREDIENT

Brucea javanica
Rhizoma coptidis
Cantharides
calamus
pepper
osthole
Phellodendron
Sophora flavescens
camphor
borneol
glycerin
ethanol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TAG WART REMOVER 
salicylic acid 10% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84735-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	10 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LYTTA VESICATORIA (UNII: 3Q034RO3BT)
ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
BORNEOL (UNII: M89NIB437X)
GLYCERIN (UNII: PDC6A3C0OX)
BRUCEA JAVANICA WHOLE (UNII: Z4CCI5NZ66)
OSTHOL (UNII: XH1TI1759C)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
COPTIS TEETA ROOT (UNII: A92YL7456Q)
PHELLODENDRON AMURENSE WHOLE (UNII: 3OZN5NGR9L)
ALCOHOL (UNII: 3K9958V90M)
BLACK PEPPER (UNII: KM66971LVF)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84735-004-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	03/19/2025

Labeler - Hengyang Chuangjiujia Trading Co., Ltd. (977292157)

Establishment
Name	Address	ID/FEI	Business Operations
Hengyang Chuangjiujia Trading Co., Ltd.		977292157	manufacture(84735-004)