FDA.reportPublic FDA data

Jock Itch Relief

Manufacturer
Meijer Distribution Inc
Effective date
2018-11-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:45:03

Label at a glance#

ProductJock Itch Relief
Active ingredientMICONAZOLE NITRATE
Label structure9 sections

Indications and uses

• proven clinically effective in the treatment of most jock itch (tinea cruris) • for effective relief of itching, burning, scaling and discomfort, and chafing associated with jock itch

Dosage and administration

• wash affected area and dry thoroughly • shake can well and spray a thin layer over affected area twice daily (morning and night) • supervise children in the use of this product • use daily for 2 weeks • if condition persists longer, ask a doctor • this product is not effective on the scalp or nails • in case of clogging, clean nozzle with a pin

Storage and handling

• store at 20-25°C (68-77°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Miconazole nitrate 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • proven clinically effective in the treatment of most jock itch (tinea cruris)
  • for effective relief of itching, burning, scaling and discomfort, and chafing associated with jock itch

Warnings

WARNINGS SECTION

For external use only

Flammable: Do not use while smoking or near heat or flame

Do not use

OTC - DO NOT USE SECTION

on children under 2 years of age unless directed by a doctor

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes
  • use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
  • contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F (49°C).

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation occurs
  • there is no improvement within 2 weeks

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

  • wash affected area and dry thoroughly
  • shake can well and spray a thin layer over affected area twice daily (morning and night)
  • supervise children in the use of this product
  • use daily for 2 weeks
  • if condition persists longer, ask a doctor
  • this product is not effective on the scalp or nails
  • in case of clogging, clean nozzle with a pin

Other information

STORAGE AND HANDLING SECTION

  • store at 20-25°C (68-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol denat., aluminum starch octenylsuccinate, isobutane, isopropyl myristate, propylene carbonate, sorbitan monooleate, stearalkonium hectorite, talc

Questions or comments?

OTC - QUESTIONS SECTION

1-800-719-9260

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to Lotrimin® active ingredient

jock itch relief

Miconazole nitrate 2%

Antifungal

Clinically Proven to Cure Most Jock Itch Fungus

POWDER SPRAY | GOES ON DRY

Relieves Itching, Burning, Scaling and Chafing

NET WT 4.6 OZ (130 g)

jock itch relief image
jock itch relief image

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41250-49741250-497-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
MICONAZOLE NITRATEVW4H1CYW1KACTIB
ALCOHOL3K9958V90MIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
ISOBUTANEBXR49TP611IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
PROPYLENE CARBONATE8D08K3S51EIACT
SORBITAN MONOOLEATE06XEA2VD56IACT
STEARALKONIUM HECTORITEOLX698AH5PIACT
TALC7SEV7J4R1UIACT

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
31ca4bbb-d1f7-4475-b747-e2b7b45c703d91278f01-e223-439d-bab9-34396b4d7b3e2024-11-05WarningsExact identifier
spl set id: 91278f01-e223-439d-bab9-34396b4d7b3e

Reported adverse events (FAERS/openFDA)#

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