DR. JOHNE SKIN TAG REMOVER- salicylic acid solution

Dr. Johne SKIN TAG REMOVER by

Drug Labeling and Warnings

Dr. Johne SKIN TAG REMOVER by is a Otc medication manufactured, distributed, or labeled by Dr.Johnes LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient:

1. Salicylic Acid 17%

PURPOSE

1. Wart, corn, and callus remover

INDICATIONS & USAGE

Uses For the removal of common

1. warts
2. corns
3. calluses

WARNINGS

For external use only

Do not use:

• on mucous membranes, or broken skin
• Do not apply to open wounds or infected skin

When using this product

Avoid contact with eyes

Stop use and ask a doctor if

• excessive irritation occurs.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions:

• Clean and dry the affected area
• Apply a thin layer once or twice daily
• Do not apply to open wounds or infected skin

OTHER SAFETY INFORMATION

Other information:

• Store at room temperature
• Avoid heat and direct sunlight

INACTIVE INGREDIENT

Inactive ingredients:

• Menthol
• Coptis chinensis extract (COPTIS CHINENSIS ROOT)
• Phellodendron extract (PHELLODENDRON CHINENSIS BARK)
• Acorus gramineus extract (ACORUS GRAMINEUS ROOT)
• Ethanol (ALCOHOL)
• Water (WATER)

QUESTIONS

Questions or comments?

support@drjohnes.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR. JOHNE SKIN TAG REMOVER 
salicylic acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85818-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	170 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Menthol (UNII: L7T10EIP3A)
COPTIS CHINENSIS ROOT (UNII: CXS4LJR7EL)
PHELLODENDRON CHINENSIS BARK (UNII: 2866QMZ434)
ACORUS GRAMINEUS ROOT (UNII: Z60N6Q6E19)
ALCOHOL (UNII: 3K9958V90M)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85818-001-02	7 mL in 1 TUBE; Type 0: Not a Combination Product	06/02/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	06/02/2025

Labeler - Dr.Johnes LLC (120317781)

Registrant - Dr.Johnes LLC (120317781)