WART REMOVER by Consilii LLC 83299-007 Completed

WART REMOVER by

Drug Labeling and Warnings

WART REMOVER by is a Otc medication manufactured, distributed, or labeled by Consilii LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WART REMOVER- wart remover liquid 
Consilii LLC

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83299-007 Completed

Active Ingredient

salicylic acid 12%

Purpose

Wart remover

Use

for the removal ot common and plantar warts
the common wart ls 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

When Using

avoid contact with eyes. If the product gets into the
eye lush with water for 15 minutes
avoid inhaling vapers
cap the bottle tightly

Stop Use

If discomfort persists

Ask Doctor

If you have diabetes or poor blood circulation

Keep Oot Of Reach Of Children

Keep Oot Of Reach Of Children

Directions

wash the affected area
mey soak the wart in warm water tor 5 minutes
Gry area thoroughly
using the applicator(cotton swab), apply a layer at
Gintment to sufficiently cover each wart
allow it to fully absorb and cover it with a bandage as
needed.
repeat this procedure once or twice daily as needed
(until the wart is removed) for up to 12 weeks

Inactive ingredients

Watery, Sodiurn bicarbonate
Propylene glycol, Ethanol, Frutus cnidil,
Kuhrseng, Pursiane, The rhizome of
large-headed atractylodes, Radix angelicae,
Pericarpiur citri reticulatae, Asarum,
Fructus forsythiae, Bamboo leat, Platycodon
grandiflorur, xanthan gum

PRINCIPAL DISPLAY PANEL

WART REMOVER 
wart remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83299-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	12 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SURINAMINE (UNII: AIQ58N56TM)
PURSLANE (UNII: M6S840WXG5)
ATRACTYLODES LANCEA WHOLE (UNII: HT7Q1X5HVM)
CITRUS MAXIMA FRUIT RIND (UNII: 5NX3G75CA6)
FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5)
BAMBUSA VULGARIS LEAF (UNII: EMY54R518C)
PLATYCODON GRANDIFLORUS WHOLE (UNII: WC73QE9274)
XANTHAN GUM (UNII: TTV12P4NEE)
CNIDIUM MONNIERI WHOLE (UNII: GYR30735RE)
PLATYCODON GRANDIFLORUM LEAF (UNII: 2L64H2X8DY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83299-007-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	06/13/2023	08/29/2024

Labeler - Consilii LLC (118891890)

Establishment
Name	Address	ID/FEI	Business Operations
Consilii LLC		118891890	manufacture(83299-007) , label(83299-007)

Revised: 8/2024

Document Id: 20d164b6-ab93-4297-e063-6394a90a0df7

34390-5

Set id: fe0611db-7adf-9678-e053-6294a90a1153

Version: 2

Effective Time: 20240829

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