Active Ingredient
SALICYLIC ACID 10%
Warticide Solution
FDA Label NDC 71229-105
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Sisquoc Healthcare Corporation for the product Warticide (NDC 71229-105). 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, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
0-image_warticide_front (0 Image Warticide Front)
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