Indications and uses
Uses for the removal of corns and calluses relieves pain by removing corns and calluses
Uses for the removal of corns and calluses relieves pain by removing corns and calluses
Directions wash affected area and dry thoroughly apply one drop at a time with applicator to sufficiently cover each corn/callus let dry repeat procedure once or twice daily as needed for up to 14 days (until corn/callus is removed) may soak corn/callus in warm water for 5 minutes to assist in removal protective pads may be used to cushion corn/callus during treatment
Drug Facts
Active Ingredient Purpose
Salicylic Acid 17%w/w.......................Corn and callus remover
Corn and callus remover
Uses
for the removal of corns and calluses
relieves pain by removing corns and calluses
Warnings
For external use only
Flammable: Keep away from fire or flames.
Do not use
if you are a diabetic
if you have poor blood circulation
on irritated skin or any area that is infected or reddened
When using this product
if product gets in eyes, flush with water for 15 minutes
do not inhale vapors
cap bottle tightly and store at room temperature away from heat
Stop use and ask a doctor if discomfort lasts
Keep out of reach of children. If swallowed,
get medical help or contact a Poison Control Center right away.
Directions
wash affected area and dry thoroughly
apply one drop at a time with applicator to sufficiently cover each corn/callus
let dry
repeat procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)
may soak corn/callus in warm water for 5 minutes to assist in removal
protective pads may be used to cushion corn/callus during treatment
Other information
store between 20ºC to 25ºC (68º to 77ºF)
keep tightly closed
retain card for full labeling
Inactive ingredients castor oil, ethyl lactate, flexible collodion, polybutene. (Contains alcohol 18% v/v and ether 53% v/v from flexible collodion)
Questions? 1-866-360-3226
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 66843-046 | 66843-046-41 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ETHER | 0F5N573A2Y | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| ETHYL LACTATE | F3P750VW8I | IACT |
| SALICYLIC ACID | O414PZ4LPZ | ACTIB |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| d672cdb2-6cb3-53ee-e053-2995a90a41a7 | d672d35a-6a06-362f-e053-2995a90a9ce1 | 2022-01-25 | Warnings | d672cdb2-6cb3-53ee-e053-2995a90a41a7 d672d35a-6a06-362f-e053-2995a90a9ce1 |
Adverse event summaries are temporarily unavailable. Other product information remains available.