DR. JOHNES LIQUID SKIN WART CORN REMOVER- salicylic acid solution

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient:

1. Salicylic Acid 17%

PURPOSE

1. Wart Remover

INDICATIONS & USAGE

Uses:

• Plantar Warts
• Common Warts
• Flat Warts
• Corns in Big Toes
• Corns in Heels
• Corns on Feet
• Corns on Hands
• Any Other Spot

WARNINGS

For external use only

Do not use:

• Face
• Genital warts
• Moles
• Birthmarks
• Open wounds
• Irritated skin
• Infected skin
• Mucous membranes

Ask a doctor before use if you have diabetes or poor blood circulation.

Stop use and ask a doctor if

• discomfort, burning, redness or irritation occurs.

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION

Directions:

1. Wash and dry the affected area.
2. Apply a small amount directly to the wart, corn or callus.
3. Allow the liquid to dry and form a protective film.
4. Repeat as directed until removed.
5. For best results, use consistently as part of your daily care routine.
6. The liquid formula dries into a protective film to help keep treatment in place.
7. Use only as directed.

INACTIVE INGREDIENT

Inactive Ingredients:

• Water (Aqua)
• Aloe Barbadensis Leaf Juice
• Glycerin
• Citrus Aurantium Dulcis (Orange) Peel Extract
• Menthol
• Propolis Extract
• Bee Venom
• Echinacea Purpurea Extract
• Tea Tree Oil
• Calendula Officinalis Extract
• Gotu Kola Extract
• Turmeric Extract (Curcuma Longa)
• Caprylyl Glycol
• Sodium Benzoate
• Potassium Sorbate
• Xanthan Gum
• Lecithin

QUESTIONS

Questions or comments?

support@drjohnes.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR. JOHNES LIQUID SKIN WART CORN REMOVER 
salicylic acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85818-003
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
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
GLYCERIN (UNII: PDC6A3C0OX)
ORANGE PEEL (UNII: TI9T76XD44)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
APIS MELLIFERA VENOM (UNII: 76013O881M)
ECHINACEA PURPUREA WHOLE (UNII: QI7G114Y98)
TEA TREE OIL (UNII: VIF565UC2G)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
TURMERIC (UNII: 856YO1Z64F)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
XANTHAN GUM (UNII: TTV12P4NEE)
LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85818-003-01	20 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	05/22/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	05/22/2026

Labeler - Dr.Johnes LLC (120317781)

Registrant - Dr.Johnes LLC (120317781)