MAXIMUM STRENGTH WART REMOVER PATCHES- salicylic acid patch

Maximum Strength Wart Remover Patches by

Drug Labeling and Warnings

Maximum Strength Wart Remover Patches by is a Otc medication manufactured, distributed, or labeled by Henan Toudaorong Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Salicylic acid 30%
Purpose Wart remove

KEEP OUT OF REACH OF CHILDREN

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

PURPOSE

For the removal of common warts and plantar warts.Common warts arerough, cauliflower-like growths often on fingers/hands. Plantar wartsoccur on the soles of feet.

WARNINGS

Warnings

Do not use on face, genital warts, moles with hair, or irritated/reddened skin

INACTIVE INGREDIENT

Inactive ingredients Cellulose Gum, Propylene Glycol, Cyclodextrin, MelaleucaAlternifolia (Tea Tree) Leaf Oil, Centella Asiatica Extract, Polvisobutene.Hvdroxvethylcelulose,Disodium Phosphate, polysorbate 60
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INDICATIONS & USAGE

on irritated skin or any area that is infected or reddened"

on moles, birthmarks, warts with hair growing from them, genital warts, or wartson the face or mucous membranes,

DOSAGE & ADMINISTRATION

Directions

wash afected areadry area thoroughly apply the patch directly over the wart or tagrepeat this procedure every 48 hours as needed, until the wart or tag is removedf崧or up to 12 weeks"Apply the procedure every 48 hours, up to 12 weeks, until the wart isremoved.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MAXIMUM STRENGTH WART REMOVER PATCHES 
salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85136-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	30 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 60 (UNII: CAL22UVI4M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5)
CELLULOSE GUM (UNII: K679OBS311)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
DISODIUM PHOSPHATE (UNII: 22ADO53M6F)
CYCLODEXTRIN (UNII: 7E6SK9QDT8)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85136-011-01	144 in 1 BOX	11/23/2025
1		10 mg in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	11/23/2025

Labeler - Henan Toudaorong Biotechnology Co., Ltd. (724343239)

Registrant - Henan Toudaorong Biotechnology Co., Ltd. (724343239)