FDA Label for Warticide
View Indications, Usage & Precautions
Warticide Product Label
The following document was submitted to the FDA by the labeler of this product The Sisquoc Healthcare Corporation. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
SALICYLIC ACID 10%
Purpose
WART REMOVER
Uses
- WART REMOVER
Warnings
FOR EXTERNAL USE ONLY.
DO NOT USE ON CHILDREN UNDER 2 YEARS OF AGE UNLESS DIRECTED BY A DOCTOR.
WHEN USING THIS PRODUCT AVOID CONTACT WITH THE EYES. IF CONTACT OCCURS, RINSE THE EYES VERY THOROUGHLY WITH WATER.
STOP USE AND ASK A DOCTOR IF IRRITATION OCCURS OR THERE IS NO IMPROVEMENT WITHIN 4 WEEKS.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Directions
Simply unscrew the top and fill the dropper tip with liquid. Once full, apply Warticide to the wart or warts until the infected area is lightly covered with gel. Gently work Warticide into the wart with a finger and then wash hands after application is finished. Allow 3-4 minutes for the solution to absorb.
Inactive Ingredients
WATER, ETHANOL, XANTHAN GUM, MELALEUCA ALTERNIFOLIA LEAF OIL, CEDAR LEAF OIL.
Storage And Handling
Store between 20°c to 25°C (68° to 77°F)
Package Label.Principal Display Panel
* Please review the disclaimer below.