GoodSense Antifungal Miconazole Liquid Continuous Spray

Manufacturer
GEISS, DESTIN AND DUNN, INC.
Effective date
2025-10-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:41:32

Label at a glance#

ProductMiconazole nitrate
Active ingredientMICONAZOLE NITRATE
Label structure9 sections

Indications and uses

cures most athlete's foot (linea pedis), ringworm (linea corporis) and jock itch (linea cruris) relieves itching, burning and scaling

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 for athlete's foot: pay special attention to spaces 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 joc...

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 athlete's foot (linea pedis), ringworm (linea corporis) and jock itch (linea cruris)
  • relieves itching, burning and scaling

Warnings

WARNINGS SECTION

For external use only.

Extremely flammable:

SAFE HANDLING WARNING SECTION

Contents under pressure. Keep away from fire, sparks, and heated surfaces. Do not puncture or incinerate container. Exposure to temperatures above 120ºF may cause burning, intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

Do not use

WARNINGS 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 or mouth
  • use only as directed

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation occurs
  • no improvement within 4 weeks for athlete's foot and ringworm, and 2 weeks for jock itch

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
  • for athlete's foot: pay special attention to spaces 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 conditions persists longer, consult a doctor
  • this product is not effective on the scalp or nails

Other information

OTHER SAFETY INFORMATION

store between 20º and 30ºC (68º and 86ºF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

acetone, ethoxdiyglycol, propylene glycol, SD alcohol 40-B, tocopheryl acetate

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GOODSENSE

Anti-

Fungal

Continuous Liquid Spray

Miconazole Nitrate 2%

Liquid Countinuous Spray

  • Cures most athlete's foot
  • Relieves itching, scaling & burning

NET WT. 5.3 OZ (150g)

sprayspray

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
998533miconazole nitrate 2 % Topical SprayPSN4
998533miconazole nitrate 20 MG/ML Topical SpraySCD4
998533miconazole nitrate 2 % Topical SpraySY4
998533miconazole nitrate 3 GM in 150 GM Topical SpraySY4

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
BarcodeEAN-130846036003529GTIN-13: 0846036003529
EAN-13: 0846036003529
GTIN-12: 846036003529
UPC-A: 846036003529
GTIN storage (14 digits): 00846036003529
Good Sense_Antifungal Miconazole Continuous Liquid Spray_50-069GS-01_Updated.jpg

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50804-136-53Miconazole nitrate150 g in 1 CANISTERAEROSOL, SPRAY1504

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50804-136-53GM - Gram50804-136a63659a6-6f84-4c90-b043-bb9c9f636b8912025-05-14

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50804-13650804-136-53

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32024-11-21full-release2026-06-01 00:38:45

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
Miconazole nitrateANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAYGEISS, DESTIN AND DUNN, INC.c367c2e8-5423-bf01-e053-2a95a90ab8e92025-10-30WarningsExact identifier
ndc (package): 50804-136-53
ndc (product): 50804-136
ndc11 (package): 50804013653
spl id: 42652a20-5774-7fba-e063-6294a90a9382
spl set id: c367c2e8-5423-bf01-e053-2a95a90ab8e9

Reported adverse events (FAERS/openFDA)#

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