Antifungal Powder Spray Jock Itch

Manufacturer: Wal-Mart Stores, Inc.
Effective date: 2026-01-27
Label type: HUMAN OTC DRUG LABEL
Version: 9
Source: full-release
Hydrated at: 2026-06-01 01:35:31

Label at a glance#

ProductMiconazole Nitrate

Active ingredientMICONAZOLE NITRATE

Label structure9 sections

Indications and uses

cures most jock itch (tinea cruris) relieves itching, burning 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) or as directed by a doctor supervise children in the use of this product use daily for 2 weeks; If conditions persists, consult a doctor this product is not effective on the scalp or nails

Contacts and useful links#

PhoneLabel contact1-888-287-1915

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Miconazole nitrate 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

cures most jock itch (tinea cruris)
relieves itching, burning and chafing associated with jock itch

Warnings

WARNINGS SECTION

For external use only.

Extremely Flammable:

SAFE HANDLING WARNING SECTION

Keep away from fire, sparks, and heated surfaces. Contents under pressure. Do not puncture or incinerate. Do not sore at temperature above 120°F.

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 spraying in eyes
use only as directed
intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

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.

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) or as directed by a doctor
supervise children in the use of this product
use daily for 2 weeks; If conditions persists, consult a doctor
this product is not effective on the scalp or nails

Other Information

OTHER SAFETY INFORMATION

store between 20 ^oC and 30 ^oC (68 ^o and 86 ^oF)
if nozzle clogs, clean with a pin

Inactive ingredient

INACTIVE INGREDIENT SECTION

ISOBUTANE, SD ALCOHOL 40-B, KAOLIN, ZEA MAYS (CORN) STARCH, DISTEARDIMONIUM HECTORITE

Questions?

OTC - QUESTIONS SECTION

1-888-287-1915

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

equate

ANTIFUNGAL POWDER SPRAY

Jock Itch

Miconazole Nitrate 2% /

Antifungal

Cures most jock itch
Relieves itching,

chafing & burning

Comforts & refreshes
Talc-free

NET WT. 4.6 OZ. (130 g)

carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
MICONAZOLE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0681131082242	GTIN-13: 0681131082242 EAN-13: 0681131082242 GTIN-12: 681131082242 UPC-A: 681131082242 GTIN storage (14 digits): 00681131082242	Equate_AF Miconazole Jock Itch Powder Spray_46-MPSWM-04.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3a55f4fb-5aec-4c88-0ff7-4d608ad4866a	Product name	1	20140508
5b9a7965-36d2-8412-dcaf-f76a65411611	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49035-135-46	2023-01-31	C162847	48780-1	f386c649-a0bb-0266-e053-dadaa90a7c1a	Miconazole Jock Itch Powder Spray Talc Free
49035-135-46	2023-01-31	C162847	48780-1	f386c649-a0bb-0266-e053-dadaa90a7c1a	Miconazole Jock Itch Powder Spray Talc Free
49035-135-46	2023-01-31	C162847	48780-1	f386c649-a0bb-0266-e053-dadaa90a7c1a	Antifungal Powder Spray Jock Itch
49035-135-46	2023-01-30	C162847	48780-1	f386c649-a0bb-0266-e053-dadaa90a7c1a	Miconazole Jock Itch Powder Spray Talc Free
49035-135-46	2023-01-30	C162847	48780-1	f386c649-a0bb-0266-e053-dadaa90a7c1a	Miconazole Jock Itch Powder Spray Talc Free
49035-135-46	2023-01-30	C162847	48780-1	f386c649-a0bb-0266-e053-dadaa90a7c1a	Antifungal Powder Spray Jock Itch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49035-135-46	Miconazole Nitrate	130 g in 1 PACKAGE	AEROSOL, SPRAY	130		9

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Miconazole Nitrate
Jock Itch Spray
DISTEARDIMONIUM HECTORITE
ISOBUTANE
KAOLIN
ALCOHOL
ZEA MAYS (CORN) STARCH
MICONAZOLE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49035-135	49035-135-46

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DISTEARDIMONIUM HECTORITE	X687XDK09L	IACT
ISOBUTANE	BXR49TP611	IACT
KAOLIN	24H4NWX5CO	IACT
ALCOHOL	3K9958V90M	IACT
ZEA MAYS (CORN) STARCH	O8232NY3SJ	IACT
MICONAZOLE NITRATE	VW4H1CYW1K	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
7	2025-10-29	monthly-update	2026-06-03 17:39:02
6	2024-12-16	full-release	2026-06-01 00:43:57

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Miconazole Nitrate	JOCK ITCH SPRAY	Wal-Mart Stores, Inc.	76259769-9923-4856-a160-a738bc8a72f0	2026-01-27	Warnings	Exact identifier ndc (package): 49035-135-46 ndc (product): 49035-135 ndc11 (package): 49035013546 spl id: 496575e7-1fd9-0285-e063-6394a90ac8d4 spl set id: 76259769-9923-4856-a160-a738bc8a72f0

Reported adverse events (FAERS/openFDA)#

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