Anti-Fungal Pen

Manufacturer
CVS | Product Quest Mfg
Effective date
2017-12-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:53:23

Label at a glance#

ProductAnti-Fungal Pen CVS
Active ingredientUndecylenic Acid
Label structure8 sections

Indications and uses

For the cure of most • ringworm (tinea corporis) • athlete’s foot (tinea pedis) For the relief of: • itching • scaling • cracking •burning• redness • soreness • irritation and discomforts which may accompany these conditions

Label contents#

Full prescribing information#

Active ingredient                          Purpose

OTC - ACTIVE INGREDIENT SECTION


Undecylenic Acid 25%..................Anti-fungal

Uses

INDICATIONS & USAGE SECTION

For the cure of most • ringworm (tinea corporis) • athlete’s foot (tinea pedis) For the relief of: • itching • scaling • cracking
•burning• redness • soreness • irritation and discomforts which may accompany these conditions

WARNINGS SECTION

Warnings
For external use only.
Ask a doctor before use on children under 2 years of age
When using this product avoid contact with eyes
Stop use and ask doctor if • irritation occurs • there is no improvement within 4 weeks

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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

• read all warnings and directions • use only as directed • clean the affected area with soap and water and dry
thoroughly • remove cap from pen • twist the base of the pen, with brush pointing downward, until product dispenses • apply a
thin layer of the product over the affected area twice daily (morning and night) or as directed by a doctor • 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
• for athlete's foot and ringworm, use daily for 4 weeks. if condition persists longer, consult a doctor • intended for use by normally
healthy adults only • persons under 18 years of age or those with highly sensitive or allergic skin should use only as directed by a
doctor • supervise children in the use of this product • this product is not effective on the scalp or nails

INACTIVE INGREDIENT SECTION

Inactive ingredients : Isopropyl Palmitate, Propylparaben

OTHER SAFETY INFORMATION

Other Information Store at 15°-30°C (59°-86°F) • Keep cap on pen when not in use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
998329undecylenic acid 25 % Topical SolutionPSN2
998329undecylenic acid 250 MG/ML Topical SolutionSCD2
998329undecylenic acid 25 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59779-835-012020-01-31C16284748780-19d75b9d0-6e56-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59779-835-01Anti-Fungal PenCVS1 in 1 CARTONLIQUID12
59779-835-01Anti-Fungal PenCVS1.7 mL in 1 CONTAINERLIQUID1.72

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59779-835ANTI-FUNGAL PEN CVS (UNDECYLENIC ACID) LIQUID [CVS]2Legacy NDC, 2 package rows20171212_2da74531-118f-4817-8871-50980ade6e5d.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59779-83559779-835-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML · Source PDF

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
c3e5ee58-0453-4842-a372-ae95d48236182da74531-118f-4817-8871-50980ade6e5d2017-12-12WarningsExact identifier
spl id: c3e5ee58-0453-4842-a372-ae95d4823618
spl set id: 2da74531-118f-4817-8871-50980ade6e5d

Reported adverse events (FAERS/openFDA)#

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