Kingskin Wart (K)(WP) (DA)

Kingskin by

Drug Labeling and Warnings

Kingskin by is a Otc medication manufactured, distributed, or labeled by Pharmadel LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KINGSKIN- salicylic acid liquid 
Pharmadel LLC

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Kingskin Wart (K)(WP) (DA)

Drug Facts

Active Ingredient and Purpose

• Active ingredient: Purpose
• Salicylic acid 17% w/w...................................:

  Wart remover

Use

For the removal of common warts. The common wart is easily recognized by the rough “cauliflower-like” appearance of the surface.

Warnings

Do not use

For external use only. FLAMMABLE: keep away from fire or flame.

• on irritated skin
• on any area that is infected or reddened
• if you are a diabetic
• if you have poor blood circulation
• on moles, birthmarks, warts with hair growing from them, genital warts or warts on the face
• on mucous membranes

When using this product

• cap bottle tightly
• if product gets into the eye, flush with water for 15 minutes
• avoid inhaling vapors

Stop use and ask a doctor if

discomfort persists.

KEEP OUT OF REACH OF CHILDREN.

If accidental ingestion occurs, get medical help, or contact a Poison Control Center right away.

Directions

• wash affected area
• dry area thoroughly
• apply one drop at a time with applicator to sufficiently cover each wart
• let dry
• repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks

Other information

• store at room temperature away from heat
• do not use if seal over cap is torn or missing.

Inactive ingredients

alcohol, camphor, ether

Questions or comments?

1-866-359-3478 (M-F) 9 AM -5 PM EST or www.pharmadel.com

Principal Display Panel

KINGSKIN 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55758-409
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	17 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ETHER (UNII: 0F5N573A2Y)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)

Product Characteristics
Color	yellow	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55758-409-15	1 in 1 BOX	01/17/2024	01/01/2025
1		15 mL in 1 BOTTLE, WITH APPLICATOR; 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	03/31/2021	01/01/2025

Labeler - Pharmadel LLC (030129680)

Revised: 12/2025

Document Id: 4526678c-122e-aa4d-e063-6394a90adbcf

34390-5

Set id: 09974c86-6fba-3f20-e063-6294a90abd89

Version: 6

Effective Time: 20251204