Hermon Jock Itch spray.

Manufacturer
Beautivity LLC
Effective date
2026-02-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:50:17

Label at a glance#

ProductHermon Jock Itch spray.
Active ingredientMICONAZOLE NITRATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Miconazole Nitrate 2%

OTC - PURPOSE SECTION

Antifungal

DOSAGE & ADMINISTRATION SECTION

  • Cures most athlete's foot(tinea pedis), ringworm(tinea corporis) and jock itch(tinea cruris)
  • Relieves itching, burning and scaling

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

on children under 2 of age except under the advice and supervision of a doctor.

OTC - WHEN USING SECTION

Avoid contact with the eye.

OTC - ASK DOCTOR SECTION

  • Irritation occurs
  • condition persists
  • there is no improvement of athlete's foot or ringworm within 4 weeks or jock itch within 2 weeks.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

  • Clean the affected area and dry thoroughly
  • Shake well and spray a thin layer over affected area twice daily(morning and night) or as directed by a doctor
  • Supervise children in the use of this product
  • For athlete's foot, pay special attention to the spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
  • For athlete's foot and righworm, use daily for 4 weeks
  • For jock itch, use daily for 2 weeks
  • 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

Water, Alcohol, Propylene Glycol, Chlorhexidine Digluconate, Cnidium Monnieri Fruit Extract, Cortex Dictamni Root Extract, Kochia Scoparia Fruit Extract, Mentha Haplocalyx Leaf Extract, Sophora Flavescens Root Extract,Stemona Tuberosa Root Extract

OTC - QUESTIONS SECTION

service@hermohealth.com

Tel: 573-476-4179

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
998533miconazole nitrate 2 % Topical SprayPSN1
998533miconazole nitrate 20 MG/ML Topical SpraySCD1
998533miconazole nitrate 2 % Topical SpraySY1
998533miconazole nitrate 3 GM in 150 GM Topical SpraySY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MICONAZOLE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeq-r.to/ITCHSPpackage.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3a55f4fb-5aec-4c88-0ff7-4d608ad4866aProduct name120140508
5b9a7965-36d2-8412-dcaf-f76a65411611Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85398-030-01Hermon Jock Itch spray.1 in 1 CARTONLIQUID11
85398-030-01Hermon Jock Itch spray.60 g in 1 BOTTLE, SPRAYLIQUID601

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85398-03085398-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
Hermon Jock Itch spray.MICONAZOLE NITRATE 2%Beautivity LLC4b633528-667a-f34e-e063-6294a90a2b3d2026-02-21WarningsExact identifier
ndc (package): 85398-030-01
ndc (product): 85398-030
ndc11 (package): 85398003001
spl id: 4b633528-667b-f34e-e063-6294a90a2b3d
spl set id: 4b633528-667a-f34e-e063-6294a90a2b3d

Reported adverse events (FAERS/openFDA)#

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