Peunitory Fungal Nail Treatment

Manufacturer
Guangzhou Huixue Biotechnology Co., Ltd.
Effective date
2026-03-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:50:40

Label at a glance#

ProductPeunitory Fungal Nail Treatment
Active ingredientTOLNAFTATE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

INACTIVE INGREDIENT SECTION

Aloe Vera Extract, Helianthus Annuus (Sunflower) Seed Oil, Prunus Armeniaca (Apricot) Kernel Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Eugenia Caryophyllus (Clove) Bud Oil, Lavandula Angustifolia (Lavender) Oil, Hakka Yu, Tocopherol, Origanum Vulgare Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Eucalyptol, Tocopheryl Acetate, Squalene, Propolis Extract, Citrus Bergamia (Bergamot) Fruit Oil.

OTC - PURPOSE SECTION

Antifungal

INDICATIONS & USAGE SECTION

For the treatment of nail fungus and associated symptoms, including discoloration, thickening, splitting, crumbling, and brittleness

WARNINGS SECTION

Warnings For external use only. De not use on children under 2 years of age unless directed by a doctor. When using this product, avoid contact with the eyes. tion occurs or if there is no improvement within 4 weeks. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Store at room temperature. Avoid direct sunlight.

OTC - WHEN USING SECTION

1. Clean the affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Gently file the nail to make it thinner and remove debris, being cautious not to harm the nail bed. For best results, file nails every 2-3 days. 2. Supervise children in the use of this product. For athlete's foot: Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. To prevent athlete's foot, apply once or twice daily (morning and/or night). For toe fungus, apply to skin around the nail and cuticle. Visible improvement may be seen in as little as 7 days. Continue regular use to help prevent fungus regrowth.

OTC - DO NOT USE SECTION

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. Stop use and ask a doctor if irritation occurs or if there is no improvement within 4 weeks.

OTC - STOP USE SECTION

irritation occurs or if there is no improvement within 4 weeks.

DOSAGE & ADMINISTRATION SECTION

Twice each day,(1ml)each time.7 days supply

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Peunitory Fungal Nail TreatmentPeunitory Fungal Nail Treatment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87204-169-01Peunitory Fungal Nail Treatment15 mL in 1 BOTTLE, PLASTICLIQUID151

Products#

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DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87204-16987204-169-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Peunitory Fungal Nail TreatmentTOLNAFTATE 1%Guangzhou Huixue Biotechnology Co., Ltd.4d2e86bc-5122-ba4a-e063-6394a90acf132026-03-16WarningsExact identifier
ndc (package): 87204-169-01
ndc (product): 87204-169
ndc11 (package): 87204016901
spl id: 4d2e86bc-5123-ba4a-e063-6394a90acf13
spl set id: 4d2e86bc-5122-ba4a-e063-6394a90acf13

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.