RAGKUN WART REMOVER- salicylic acid liquid

Ragkun WART REMOVER by

Drug Labeling and Warnings

Ragkun WART REMOVER by is a Otc medication manufactured, distributed, or labeled by Jiashen International Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic acid 5%

INACTIVE INGREDIENT

Borneol

Glycerin

Podofilox

Water
Polyethylene Glycol

KEEP OUT OF REACH OF CHILDREN

Keep out of Reach of children

PURPOSE

Plantar wart

Corn

Calluses

Flat warts
Common wart

WARNINGS

Warnings
For external use only. Flammable.Keep awayfrom fire and flame.Do not use on irritatedskin or on any area that is infected orreddened·on moles, birthmarks, warts withhair growing from them, genital warts or wartson the face or mucous membranes*if you havediabetes or poor blood circulation.

INDICATIONS & USAGE

avold contact wth eyes. f product gets intothe eye, ush with water for 15minutes. avoidinhalng vapors cap tighly and store at roomtemperature away from heat

DOSAGE & ADMINISTRATION

wash affected area·may soak wart in warmwater for 5 minutes· dry area thoroughly· bysqueezing tube gently, apply one drop at a timeto sufficiently cover each wart·let dry·repeatthis procedure once or twice daily as needed(until wart is removed)for up to 12 weeks

OTHER SAFETY INFORMATION

store at room temperature*avoid excessiveheat 37°C (99°F)·skin discoloration may accurduring or after use· wipe the tip of the tubewith a paper towel between uses

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RAGKUN WART REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84867-021
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
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
BORNEOL (UNII: M89NIB437X)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PODOFILOX (UNII: L36H50F353)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84867-021-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	08/20/2025

Labeler - Jiashen International Trading Co., Ltd. (989067943)

Registrant - Jiashen International Trading Co., Ltd. (989067943)