DR.JOHNES SKIN TAG REMOVER- salicylic acid solution

Dr.Johnes SKIN TAG REMOVER by

Drug Labeling and Warnings

Dr.Johnes 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. Skin Tag, 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

Available in 7 mL, 8 mL, 9 mL, and 10 mL tubes. All packages look the same externally, with the only variation being fill volume.

INGREDIENTS AND APPEARANCE

DR.JOHNES SKIN TAG REMOVER 
salicylic acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85818-002
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: 85818-002-01	10 mL in 1 TUBE; Type 0: Not a Combination Product	06/02/2025
2	NDC: 85818-002-02	9 mL in 1 TUBE; Type 0: Not a Combination Product	06/02/2025
3	NDC: 85818-002-03	8 mL in 1 TUBE; Type 0: Not a Combination Product	06/02/2025
4	NDC: 85818-002-04	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)