Label: PURESKIN FUNGAL NAIL RENEWAL PATCHES patch
- NDC Code(s): 84746-006-01
- Packager: Shandong Yuyaotang Pharmaceutical Co., Ltd
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 12, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
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Warnings
1. Keep out of children's reach. Avoid contact with eyes, mouth, mucous membranes, wounds, or inflamed skin.
2. External use only.
3. Do not use if allergic to any ingredient.
4. Do not use in children.
5. Do not use if pouch is torn or broken.
6. Discontinue use if skin becomes red, swollen, or itchy, and consult a healthcare professional. - Keep Oot Of Reach Of Children
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Directions
Begin by removing any nail polish. Cleanse nails and surrounding skin, ensuring thorough drying to enhance adhesion.
a. Peel off protective films and sequentially.
b. Apply the patch to the affected nail area, removing release paper.
c. Firmly cover the sides of the toe or finger.
d. Fold the remaining adhesive to envelop the toe/fingertip.
e. Maintain the patch for 6-8 hours (overnight use recommended for 3-6 months).
Use daily for optimal results. It is recommended to roughen the nail surface before application for better adhesion. - Other information
- Inactive ingredients
- Questions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PURESKIN FUNGAL NAIL RENEWAL PATCHES
pureskin fungal nail renewal patches patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84746-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength UNDECYLENIC ACID (UNII: K3D86KJ24N) (UNDECYLENIC ACID - UNII:K3D86KJ24N) UNDECYLENIC ACID 8 g in 100 Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) IVERMECTIN (UNII: 8883YP2R6D) DICLORAN (UNII: F0BE9UC5J7) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) POWDERED CELLULOSE (UNII: SMD1X3XO9M) ACRYLIC ACID (UNII: J94PBK7X8S) ARCHANGELENONE (UNII: AG84U27TWU) POLYESTER-7 (UNII: 0841698D2F) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84746-006-01 21 in 1 BOX; Type 0: Not a Combination Product 09/30/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 09/30/2024 12/13/2024 Labeler - Shandong Yuyaotang Pharmaceutical Co., Ltd (974645696) Establishment Name Address ID/FEI Business Operations Shandong Yuyaotang Pharmaceutical Co., Ltd 974645696 manufacture(84746-006)