87681-012 Cysndra Fungal Nail Revitalizer

Manufacturer
Guangzhou Xinhongda Trading Service Co., Ltd.
Effective date
2026-07-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
weekly-update
Hydrated at
2026-07-17 21:43:31

Label at a glance#

ProductCysndra Fungal Nail Revitalizer
Active ingredientUNDECYLENIC ACID
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Undecylenic Acid 25%

OTC - PURPOSE SECTION

Antifungal

INDICATIONS & USAGE SECTION

USE: For superficial skin fungalinfections, skin candidiasis,onychomycosis.

WARNINGS SECTION


·For external use only.
· Contraindicated for children,pregnant and lactating women.
· Prohibited for those who are allergic to this product. Allergic persons should be cautious.
· Prohibit the use ofthisproduct when the properties of the product have changed.

OTC - DO NOT USE SECTION

Do not use if there is any burning sensation, redness or swelling at the site of application.

OTC - WHEN USING SECTION


When Using this product,
avoid contact with eyes, nose, and mouth. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop Using and ask a doctor if

irritation or redness develops and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Keep out of reach of Children.
In case of accidental ingestion, get medical help or contact a poison control center immediately.

DOSAGE & ADMINISTRATION SECTION

For external use only. Use the brush to apply a layer of liquid directly to the affected nail(s),2-3 times daily for 2-4 weeks.

INACTIVE INGREDIENT SECTION

ALCOHOL
WATER
UREA
PROPYLENE GLYCOL
SALICYLIC ACID
MENTHOL
HYDROXYPROPYLCELLULOSE
ZANTHOXYLUM BUNGEANUM FRUIT EXTRACT
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL
DISODIUM EDTA
GLYCOLIC ACID

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1

Products#

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DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87681-01287681-012-01, 87681-012-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
55e9f1cf-4056-6c27-e063-6394a90ac37355e9f1cf-4055-6c27-e063-6394a90ac3732026-07-05WarningsExact identifier
spl id: 55e9f1cf-4056-6c27-e063-6394a90ac373
spl set id: 55e9f1cf-4055-6c27-e063-6394a90ac373

Reported adverse events (FAERS/openFDA)#

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