BeamBalm FUNGL NAIL

Manufacturer
Jiangxi Yudexi Pharmaceutical Co., LTD
Effective date
2026-02-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:37:11

Label at a glance#

ProductBeamBalm FUNGL NAIL
Active ingredientTOLNAFTATE
Label structure12 sections

Dosage and administration

For athlete's foot and ring worm:use daily for 4 weeks.Clean the affected area and dry thoroughly.Keep away from fire and flames.For external use on nails and the immediately adjacent skin only.Use once daily, preferably before bedtime. Unscrew the bottle cap and use the brush to apply the medicine directlyto the nail.The medication will then penetrate deeply into the nail.If the nail area is infected, spray the m...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Use

INDICATIONS & USAGE SECTION

Antifungal treatment for fingernails,toenails, and surrounding skin.Effective against fungal nails and athlete's foot caused by fungi.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

if you experience any signs of sensitivity or irritation

When Using

OTC - WHEN USING SECTION

Not for use in the eyes, mouthor vaginal area.

Stop Use

OTC - STOP USE SECTION

lf the area of application shows increased irritation lf there is Consult a doctor if symptoms worsen.If pregnant or breaslleeding

Ask Doctor

OTC - ASK DOCTOR SECTION

lf the area of application shows increased irritation lf there is Consult a doctor if symptoms worsen.If pregnant or breaslleeding

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

lf accidental ingestion occurs,seek medical assistance or contact a Poison Control Centerimmediately.

Directions

DOSAGE & ADMINISTRATION SECTION

For athlete's foot and ring worm:use daily for 4 weeks.Clean the affected area and dry thoroughly.Keep away from fire and flames.For external use on nails and the immediately adjacent skin only.Use once daily, preferably before bedtime.
Unscrew the bottle cap and use the brush to apply the medicine directlyto the nail.The medication will then penetrate deeply into the nail.If the nail area is infected, spray the medication onto the affected area.SHAKE WELL BEFORE USE.Store at 5'c to 30°0(41'F to 86°F) in a cool dry place. Keep tighosedand away from sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water ,euphorbia hirta whole, glycerin hydracrylic acid, pseudolarix amabilis bark, resorcinol.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313423tolnaftate 1 % Topical SolutionPSN1
313423tolnaftate 10 MG/ML Topical SolutionSCD1
313423tolnaftate 1 % Topical SolutionSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85248-047-01BeamBalm FUNGL NAIL4 mL in 1 TUBELIQUID41

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
85248-04785248-047-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
BeamBalm FUNGL NAILTOLNAFTATE 1% FUNGL NAILJiangxi Yudexi Pharmaceutical Co., LTD49f72e97-2393-dca8-e063-6394a90a6f102026-02-03WarningsExact identifier
ndc (package): 85248-047-01
ndc (product): 85248-047
ndc11 (package): 85248004701
spl id: 49f72e97-2394-dca8-e063-6394a90a6f10
spl set id: 49f72e97-2393-dca8-e063-6394a90a6f10

Reported adverse events (FAERS/openFDA)#

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