ProCure Antifungal

Manufacturer: Twin Med LLC
Effective date: 2025-12-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:18:45

Label at a glance#

ProductProCure Antifungal

Active ingredientMICONAZOLE NITRATE

Label structure7 sections

Indications and uses

Uses Proven clinically effective in the treatment of most athlete’s foot, jock itch and ringworm Relieves itching, scaling, cracking, burning, redness, soreness, irritation, and discomforts associated with all three treatments. Also relieves chaffing associated with jock itch.

Dosage and administration

Directions clean affected area and dry thoroughly apply thin layer of powder to 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 space between the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily. for athlete’s foot and ringworm, use daily for 4 weeks; for jock i...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Mconazole Nitrate 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

Uses

Proven clinically effective in the treatment of most athlete’s foot, jock itch and ringworm
Relieves itching, scaling, cracking, burning, redness, soreness, irritation, and discomforts associated with all three treatments. Also relieves chaffing associated with jock itch.

Warnings

WARNINGS SECTION

Warnings

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use on children under 2 years of age unless directed by a doctor

When using this product

OTC - WHEN USING SECTION

When using this product avoid contact with eyes

Stop using and ask a doctor if

OTC - STOP USE SECTION

Stop using and ask a doctor if

irritation occurs
there is no improvement within 4 weeks (for athlete’s foot or ringworm) or 2 weeks (for jock itch)

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of Children. In case of accidental ingestion, contact a physician or Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

clean affected area and dry thoroughly
apply thin layer of powder to 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 space between the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily.
for athlete’s foot and ringworm, use daily for 4 weeks; for jock itch use daily for 2 weeks
if condition persists longer, consult a doctor
this product is not effective on the scalp or nails

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Colloidal Silicon Dioxide, Corn Starch, Dipotassium Glycyrrhizinate, Sodium Benzoate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antifungal Powder Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
998461	miconazole nitrate 2 % Topical Powder	PSN	1
998461	miconazole nitrate 0.02 MG/MG Topical Powder	SCD	1
998461	miconazole nitrate 2 % Topical Powder	SY	1

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	0816516015632	GTIN-13: 0816516015632 EAN-13: 0816516015632 GTIN-12: 816516015632 UPC-A: 816516015632 GTIN storage (14 digits): 00816516015632	Antifungal Powder Image.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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55681-043-03	ProCure Antifungal	85 g in 1 BOTTLE	POWDER	85		1

Products#

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

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

ProCure Antifungal
Miconazole Nitrate 2%
MICONAZOLE NITRATE
MICONAZOLE
STARCH, CORN
SODIUM BENZOATE
GLYCYRRHIZINATE DIPOTASSIUM
SILICON DIOXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55681-043	55681-043-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MICONAZOLE NITRATE	VW4H1CYW1K	ACTIB
STARCH, CORN	O8232NY3SJ	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
GLYCYRRHIZINATE DIPOTASSIUM	CA2Y0FE3FX	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ProCure Antifungal	MICONAZOLE NITRATE 2%	Twin Med LLC	3d375325-ddad-f1e1-e063-6394a90a679f	2025-12-01	Warnings	Exact identifier ndc (package): 55681-043-03 ndc (product): 55681-043 ndc11 (package): 55681004303 spl id: 3d375325-ddae-f1e1-e063-6394a90a679f spl set id: 3d375325-ddad-f1e1-e063-6394a90a679f

Reported adverse events (FAERS/openFDA)#

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