Active Ingredient
Salicylic acid 40%w/w
Salicylic Acid
FDA Label NDC 56104-047
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Premier Brands Of America Inc. for the product Salicylic Acid (NDC 56104-047). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, keep out of reach of children, otc - stop use, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Corn remover
Use
- for the removal of corns
Warnings
For external use only.
Do Not Use
- if you are a diabetic
- have poor blood circulation
- on irritated skin or any area that is infected or reddened
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Otc - Stop Use
If discomfort persists see your doctor or podiatrist.
Directions
- wash affected area: may soak corn in warm water for 5 minutes
- dry area thoroughly
- remove bandage strips by peeling backing off at slit
- carefully adhere bandage with the medicated portion directly over corn
- after 48 hours remove medicated bandage strip
- repeat this procedure every 48 hours as needed (until corn is removed) for up to 14 days
Other Information
store between 59° to 86°F (15° to 30°C)
Inactive Ingredients
acrylic adhesive, brown iron oxide, polyethylene foam
Questions?
call 1-866-964-0939
Principal Display Panel
Premier
Medicated
ONE-STEP CORN
REMOVERS
Salicylic Acid
Effective corn removal treatment
Medicated bandage conceals & protects
One-step, no mess application
Tan Bandage
8 Medicated Bandages
* Please review the disclaimer below.
