Hermon Jock Itch Antifungal Treatment .Soap. Bar

Manufacturer
Beautivity LLC
Effective date
2026-03-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:51:10

Label at a glance#

ProductHermon Jock Itch Antifungal Treatment .Soap. Bar
Active ingredientTOLNAFTATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

OTC - PURPOSE SECTION

Antifungal

DOSAGE & ADMINISTRATION SECTION

Helps relieve and prevent itching, burning, cracking, and scaling associated with fungal infections such as jock itch, athlete's foot, ringworm, and other skin irritations.

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

Avoid contact with the eye.

OTC - STOP USE SECTION

Stop and ask a doctor if irritation occurs or if there is no improvement within 2 weeks for jock itch or within 4 weeks for athlete's foot and ringworm.

OTC - DO NOT USE SECTION

Do not use on children under 2 years ofage unless directed by a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

  • Wash affected area well and let product sit 2-3 minutes beforerinsing.
  • Make sure to dry affected area thoroughly.
  • Supervise children in theuse of this product.
  • For Athlete's foot: pay special attention to the spacesbetween the toes; wear well-fitting, ventilated shoes and change shoes andsocks at least once daily.
  • Use 1-2 times daily. Use daily for 4 weeks; if conditionpersists longer, ask a doctor.
  • This product is not effective on the scalp or nails.

OTHER SAFETY INFORMATION

Store at room temperature 59°-86°F (15°-30°C)

INACTIVE INGREDIENT SECTION

Sucrose, Stearic Acid, Propylene Glycol, Sorbitol,Sodium Palmitate, Water, Glycerin, Butyrospermum Parkii (Shea) Butter,Lauric Acid, Sodium Hydroxide, Melaleuca Alternifolia (Tea Tree) Leaf Oil,Aloe Barbadensis Leaf Juice, Cocos Nucifera (Coconut) Oil, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1807715tolnaftate 1 % Medicated Bar SoapPSN1
1807715tolnaftate 0.01 MG/MG Medicated Bar SoapSCD1
1807715tolnaftate 1 % Medicated Bar SoapSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130199874918068GTIN-13: 0199874918068
EAN-13: 0199874918068
GTIN-12: 199874918068
UPC-A: 199874918068
GTIN storage (14 digits): 00199874918068
package.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85398-031-01Hermon Jock Itch Antifungal Treatment .Soap. Bar113 g in 1 CARTONSOAP1131
85398-031-02Hermon Jock Itch Antifungal Treatment .Soap. Bar226 g in 1 CARTONSOAP2261

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85398-03185398-031-01, 85398-031-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hermon Jock Itch Antifungal Treatment Kit Antifungal Cream and .Soap. for Jock ItchANTIFUNGAL TREATMENT KITBeautivity LLC4800a93b-7042-827b-e063-6294a90acd952026-03-25WarningsExact identifier
ndc (package): 85398-031-01
ndc11 (package): 85398003101
Hermon Jock Itch Antifungal Treatment .Soap. BarTOLNAFTATE 1%Beautivity LLC4dbbf09b-5bc1-501b-e063-6394a90a2a9d2026-03-23WarningsExact identifier
ndc (package): 85398-031-01
ndc (package): 85398-031-02
ndc (product): 85398-031
ndc11 (package): 85398003101
ndc11 (package): 85398003102
spl id: 4dbbf09b-5bc2-501b-e063-6394a90a2a9d
spl set id: 4dbbf09b-5bc1-501b-e063-6394a90a2a9d

Reported adverse events (FAERS/openFDA)#

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