Dr.Johnes Liquid Skin Wart Corn Remover

Manufacturer
Dr.Johnes LLC
Effective date
2026-05-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-08-04 03:34:00

Label at a glance#

ProductDr.Johnes Liquid Skin Wart Corn Remover
Active ingredientSalicylic Acid
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient:

  1. Salicylic Acid 17%

OTC - PURPOSE SECTION

  1. Wart Remover

INDICATIONS & USAGE SECTION

Uses:

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

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use:

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

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • discomfort, burning, redness or irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION SECTION

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 SECTION

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

OTC - QUESTIONS SECTION

Questions or comments?

support@drjohnes.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package of Dr. Johnes® Liquid Skin Wart Corn Remover 17% Salicylic Acidpackage of Dr. Johnes® Liquid Skin Wart Corn Remover 17% Salicylic Acid

package of Dr. Johnes® Liquid Skin Wart Corn Remover 17% Salicylic Acidpackage of Dr. Johnes® Liquid Skin Wart Corn Remover 17% Salicylic Acid

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128X0053TGWAVdr-johnes-wart-remover-1.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85818-00485818-004-01, 85818-004-02, 85818-004-03, 85818-004-04, 85818-004-05, 85818-004-06

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32026-05-22weekly-update2026-07-17 21:43:33
22026-05-22full-release2026-06-01 01:59:04
12026-05-22weekly-update2026-06-03 18:03:04

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dr.Johnes Liquid Skin Wart Corn RemoverSALICYLIC ACIDDr.Johnes LLCf9efe02a-abc9-4a2f-afb0-9d358fc35c912026-05-22WarningsExact identifier
ndc (package): 85818-004-01
ndc (package): 85818-004-05
ndc (package): 85818-004-06
ndc (package): 85818-004-03
ndc (package): 85818-004-04
ndc (package): 85818-004-02
ndc (product): 85818-004
ndc11 (package): 85818000406
ndc11 (package): 85818000405
ndc11 (package): 85818000404
ndc11 (package): 85818000402
ndc11 (package): 85818000401
ndc11 (package): 85818000403
spl id: faae55c8-da42-4ee6-8717-6c177e7271eb
spl set id: f9efe02a-abc9-4a2f-afb0-9d358fc35c91

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.