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Ibealee wart remover - Medication Information

Product NDC Code 83675-014
Drug Name

Ibealee wart remover

Type Brand
Active Ingredients
Salicylic acid 40 g/1001
Route TOPICAL
Dosage Form PATCH
RxCUI drug identifier 240559
Application Number part358B
Labeler Name Guangzhou Hanhai Trading Co., Ltd
Packages
Package NDC Code Description
83675-014-01 144 patch in 1 patch (83675-014-01)
83675-014-02 180 patch in 1 patch (83675-014-02)
83675-014-03 540 patch in 1 patch (83675-014-03)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Salicylic Acid 40%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Apply gently to skin

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Tea Tree Oil,Calendula,Cica Oil,Castor Oil, Argan Oil

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use How to use: Directions • wash affected area and dry thoroughly • apply tag patch • after 24 hours, remove tag patch • repeat procedure every 24 hours for up to 14 days for tags /warts removal and up to 12 weeks for warts, until the problem hascleared. • may hot compress wart in warm water for 5 minutes to assist in removal

Purpose

Information about the drug product’s indications for use.
Purpose WART REMOVER

Spl product data elements

Usually a list of ingredients in a drug product.
iBeaLee WART REMOVER WART REMOVER OITICICA OIL TEA TREE OIL SALICYLIC ACID SALICYLIC ACID CALENDULA OFFICINALIS FLOWER CASTOR OIL ARGAN OIL

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PRINCIPAL DISPLAY PANEL 01 02 03

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use If allergy occurs, please stop using it

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep Oot Of Reach Of Children Do not place this product within the reach of children

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Caution: 1. Not recommended to be used simuitaneously with other medication. 2. If skin becomes red and swollen, or if burning, aching and other forms of irritation occur, cease using and seek medical advice at once. 3. It is normal to find bubbles in the colloid. 4. Keep out of reach of chidren.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API