A2A Anti-Fungal Powder

Manufacturer
A2A Integrated Pharmaceuticals, LLC
Effective date
2023-12-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:16:30

Label at a glance#

ProductA2A Anti-Fungal Powder
Active ingredientMICONAZOLE NITRATE
Label structure13 sections

Indications and uses

for the cure of most athlete's foot, jock itch, and ringworm

Dosage and administration

clean the affected area & 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, & change shoes & socks at least once daily for athlete's foot & ringworm, use daily for 4 weeks; for jock i...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Miconazole nitrate 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

for the cure of most athlete's foot, jock itch, and ringworm

Warnings

WARNINGS SECTION

For external use only.

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation occurs or there is no improvement within 4 weeks for athletes foot and ring worm, or 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

  • clean the affected area & 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, & change shoes & socks at least once daily
  • for athlete's foot & 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 scalp or nails

Other information

OTHER SAFETY INFORMATION

  • store between 20 o - 25 oC (68 o - 77 oF)
  • lightly shake bottle to loosen settled powder

Inactive ingredients

INACTIVE INGREDIENT SECTION

SODIUM ACRYLATES CROSSPOLYMER-2, ALDIOXA, CHLOROXYLENOL, IMIDUREA, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, CROSCARMELLOSE SODIUM, FRAGRANCE

Questions or comments?

OTC - QUESTIONS SECTION

call 800-380-6709 M-F 9 AM to 5 PM

Distributed by:A2A Integrated Pharmaceuticals, LLC, Bowling Green, KY 42101

This product is not manufactured or distributed by Stiefel Laboratories, Inc, owner of the registered trademark Zeasorb®

Principal Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

73141-225-80

Compare to the active ingredient in Zeasorb®

A2A INTEGRATED PHARMACEUTICALS

Moisture Absorbing

Antifungal Powder

MICONAZOLE NITRATE 2%

Relieves chafing, itching, burning & scaling

Cures & soothes most:

  • Athlete's foot
  • Jock itch
  • Ringworm

NET WT 3 OZ (85 g)

Label ImageLabel Image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73141-225-802024-01-30C16284748780-11030e365-5cb4-111a-e063-dadaa90a10e2ce2d55c0-1be6-469c-e053-2995a90a21d5

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
73141-22573141-225-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
24b97068-8d9d-880f-e063-6394a90a9f9ece2d55c0-1be6-469c-e053-2995a90a21d52024-10-18WarningsExact identifier
spl set id: ce2d55c0-1be6-469c-e053-2995a90a21d5

Reported adverse events (FAERS/openFDA)#

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