FDA.reportPublic FDA data

QQE Nail Fungus Treatment

Manufacturer
Hainan Shengtaizhuo International Information Development Co., LTD
Effective date
2025-10-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:38:06

Label at a glance#

ProductQQE Nail Fungus Treatment
Active ingredientUNDECYLENIC ACID
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Undecylenic Acid 25%

OTC - PURPOSE SECTION

Nail treatment

INDICATIONS & USAGE SECTION

Apply the treatment to the affected area of the nails

WARNINGS SECTION

For external use only.For external use only Keep away from fire and flame

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

1. Do not apply on other parts of the body
2. Avoid contact with the eyes in case of accidental contact rinse eyes with large arnounts of cool tap water.

OTC - DO NOT USE SECTION

You ae under 18 years of age, Do not use it on babies and children your scalp is red.inflamed.infected, irritated, or painful
You use other medicines .Ask a doctor before use if you hace heart disease.

OTC - STOP USE SECTION

Chest pain, rapid heart beat, faintness, or dizziness occurs sudden, unexplained weight gain occurs,your hands or feet swell.

DOSAGE & ADMINISTRATION SECTION

Twice each day,4 sprays (1ml)each time. 15 days supply

INACTIVE INGREDIENT SECTION

Aloe Vera Extract, Helianthus Annuus (Sunflower) Seed Oil, Cyclopentasiloxane, 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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Nail Fungus TteatmentNail Fungus Tteatment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84556-426-01QQE Nail Fungus Treatment30 g in 1 BOTTLE, PLASTICLIQUID302
84556-426-02QQE Nail Fungus Treatment60 g in 1 BOTTLE, PLASTICLIQUID602

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84556-42684556-426-01, 84556-426-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
EUGENIA CARYOPHYLLUS (CLOVE) BUD OIL578389D6D0IACT
LAVANDULA ANGUSTIFOLIA (LAVENDER) OILZBP1YXW0H8IACT
UNDECYLENIC ACIDK3D86KJ24NACTIB
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
TOCOPHEROLR0ZB2556P8IACT

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
408e4b9b-a2a1-0365-e063-6294a90a89f63f9c682a-f9e6-b11c-e063-6394a90a1dcd2025-10-07WarningsExact identifier
spl id: 408e4b9b-a2a1-0365-e063-6294a90a89f6
spl set id: 3f9c682a-f9e6-b11c-e063-6394a90a1dcd

Reported adverse events (FAERS/openFDA)#

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