Conazol Cream

Manufacturer
Laboratorios Liomont, S.A. de C.V.
Effective date
2025-07-07
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:06:38

Label at a glance#

ProductConazol
Active ingredientMICONAZOLE NITRATE
Label structure13 sections

Indications and uses

effective in the treatment of most athlete's foot, jock itch and ringworm relieves itching, cracking, burning and discomfort associated with these conditions

Dosage and administration

wash the affected area and dry thoroughly apply a thin layer of the product 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 the athlete's foot and ringworm, use daily for 4 weeks f...

Storage and handling

store at 20° to 25°C (68° to 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

  • effective in the treatment of most athlete's foot, jock itch and ringworm
  • relieves itching, cracking, burning and discomfort associated with these conditions

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on children less than 2 years of age unless directed by a doctor

When using this product

OTC - WHEN USING SECTION

• avoid contact with the eyes

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

  • irritation occurs
  • there is no improvement of athlete's foot or ringworm within 4 weeks or jock itch 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 the affected area and dry thoroughly
  • apply a thin layer of the product 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 the athlete's foot and ringworm, use daily for 4 weeks
  • for jock itch, use daily for 2 weeks
  • not effective on the scalp or nails

Other Information

STORAGE AND HANDLING SECTION

  • store at 20° to 25°C (68° to 77°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

butylated hydroxyanisole, caprylic/capic triglyceride,carbomer 980, emulsifying wax, glycerin, methylparaben, propylene glycol, propylparaben, purified water, triethanolamine

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label​

Sample Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2121948Conazol Antifungal 2 % Topical CreamPSN8
998483miconazole nitrate 2 % Topical CreamPSN8
2121948miconazole nitrate 20 MG/ML Topical Cream [Conazol Miconazole]SBD8
998483miconazole nitrate 20 MG/ML Topical CreamSCD8
2121948Conazol Antifungal 2 % Topical CreamSY8
2121948Conazol Miconazole 20 MG/ML Topical CreamSY8
998483miconazole nitrate 2 % Topical CreamSY8

DailyMed Pharmacologic Classes#

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

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
59208-001-02Conazol2 g in 1 TUBECREAM28
59208-001-02Conazol1 in 1 PACKAGECREAM18
59208-001-03Conazol3 g in 1 TUBECREAM38
59208-001-03Conazol1 in 1 PACKAGECREAM18
59208-001-30Conazol30 g in 1 TUBECREAM308

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59208-00159208-001-30, 59208-001-02, 59208-001-03

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
ConazolMICONAZOLE NITRATELaboratorios Liomont, S.A. de C.V.84780538-8618-5750-e053-2a91aa0a60542025-07-07WarningsExact identifier
ndc (package): 59208-001-02
ndc (package): 59208-001-03
ndc (package): 59208-001-30
ndc (product): 59208-001
ndc11 (package): 59208000130
ndc11 (package): 59208000103
ndc11 (package): 59208000102
spl id: 3958bbc4-40ed-5fe9-e063-6394a90aa502
spl set id: 84780538-8618-5750-e053-2a91aa0a6054

Reported adverse events (FAERS/openFDA)#

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