WART REMOVER- wart remover liquid 
Consilii LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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83299-001
WART REMOVER

Active Ingredient(s)

Salicylic acid 12%

Purpose

Wart remover

Use

for the removal of common and plantar warts
the common wart is easily recognized by the rough "cauliflower-like" appearance of the surface
the plantar wart is recognized by its location only on the bottom of the foot, its tenderness and the interruption of the footprint pattern

Warnings

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

Do not use

on irritated skin or on any area that is infected or reddenede
on moles, birthmarks, warts with hair growing from them, warts on the face or mucous membranes

avoid contact with eyes. If the product gets into the eye,flush with water for 15 minutes
avoid inhaling vapors
cap the bottle tightly
out of direct sunlight and store at room temperature away from heat

if discomfort persists.
if you have diabetes or poor blood circulation.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

wash the affected area
may soak the wart in warm water for 5 minutes
dry area thoroughly
using the applicator(brush or cotton swab), apply one drop at a time to sufficiently cover each wart
allow it to fully absorb and let dry
repeat this procedure once or twice daily as needed (until the wart is removed) for up to 12 weeks

Other information

Keep away from direct sunlight or heat.

Store at room tempetature 15°-30°C (59°-86°F)

Inactive ingredients

Cnidium monnieri, Podophyllum, Hawthorn, Stellera chamaejasm, Sophora flavescens, Earthy hibiscus bark, Honeysuckle

Stop use and ask a doctor

if discomfort persists.
if you have diabetes or poor blood circulation.

1-914-608-1258

Package Label - Principal Display Panel

83299-001-01

WART REMOVER 
wart remover liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83299-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE12 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
LONICERA CONFUSA FLOWER (UNII: 3JV904IJ0V)  
SOPHORA PACHYCARPA WHOLE (UNII: 4E0W7M7OOQ)  
AGERATINA HERBACEA WHOLE (UNII: 1VI0ZA82GD)  
PODOPHYLLUM HEXANDRUM ROOT (UNII: 4YOL15R9R8)  
PSEUDOLARIX AMABILIS BARK (UNII: 49G13A93VE)  
HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36)  
THYME (UNII: CW657OBU4N)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83299-001-0115 mL in 1 BOTTLE; Type 0: Not a Combination Product02/15/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM02802/15/2023
Labeler - Consilii LLC (118891890)
Establishment
NameAddressID/FEIBusiness Operations
Consilii LLC118891890manufacture(83299-001) , label(83299-001)

Revised: 5/2023
Document Id: faa303ee-60bb-726f-e053-6394a90a49c0
Set id: f57c1dd5-3ac6-8e1f-e053-2995a90ac886
Version: 2
Effective Time: 20230501
 
Consilii LLC