Dr.Johnes SKIN TAG REMOVER

Manufacturer
Dr.Johnes LLC
Effective date
2025-06-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
weekly-update
Hydrated at
2026-07-17 21:43:29

Label at a glance#

ProductDr.Johnes SKIN TAG REMOVER
Active ingredientSalicylic Acid
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient:

  1. Salicylic Acid 17%

OTC - PURPOSE SECTION

  1. Skin Tag, Wart, corn, and callus remover

INDICATIONS & USAGE SECTION

Uses For the removal of common

  1. warts
  2. corns
  3. calluses

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use:

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

OTC - WHEN USING SECTION

When using this product

Avoid contact with eyes

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • excessive 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:

  • 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 SECTION

Inactive ingredients:

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

OTC - QUESTIONS SECTION

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.

package1 of 10 mlpackage1 of 10 ml

package2 of 10 mlpackage2 of 10 ml

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128X004OE873Limg1_10ml.jpg

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85818-00285818-002-01, 85818-002-02, 85818-002-03, 85818-002-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-06-18full-release2026-06-01 01:59:01
12025-06-18monthly-update2026-06-03 17:40:04

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 SKIN TAG REMOVERSALICYLIC ACIDDr.Johnes LLCb731c55e-31ee-429f-8432-fac7c5718d832025-06-18WarningsExact identifier
ndc (package): 85818-002-04
ndc (package): 85818-002-02
ndc (package): 85818-002-03
ndc (package): 85818-002-01
ndc (product): 85818-002
ndc11 (package): 85818000203
ndc11 (package): 85818000201
ndc11 (package): 85818000202
ndc11 (package): 85818000204
spl id: 5cf5a2d4-b4c6-4ae9-83b2-f619ccef711d
spl set id: b731c55e-31ee-429f-8432-fac7c5718d83

Reported adverse events (FAERS/openFDA)#

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