SKIN PROTECTOR WITH BREATHABLE BARRIER

Manufacturer
DIVERSIFIED MANUFACTURING CORP
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:13:24

Label at a glance#

ProductSKIN PROTECTOR WITH BREATHABLE BARRIER
Active ingredientMICONAZOLE NITRATE
Label structure11 sections

Indications and uses

FOR THE TREATMENT AND PREVENTION OF: ATHLETE'S FOOT JOCK ITCH RINGWORM RELIEVES ITCHING, SCALING, CRACKING AND DISCOMFORT ASSOCIATED WITH THESE CONDITIONS.

Dosage and administration

CLEANSE AFFECTED AREA AND DRY THOROUGHLY. APPLY A THIN LAYER TO AFFECTED AREA TWICE DAILY OR AS DIRECTED BY A PHYSICIAN. FOR JOCK ITCH USE DAILY FOR TWO WEEKS. FOR ATHLETE'S FOOT AND RINGWORM USE DAILY FOR FOUR WEEKS.

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 TREATMENT AND PREVENTION OF:

  • ATHLETE'S FOOT
  • JOCK ITCH
  • RINGWORM

RELIEVES ITCHING, SCALING, CRACKING AND DISCOMFORT ASSOCIATED WITH THESE CONDITIONS.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

AVOID CONTACT WITH EYES. IN CASE OF CONTACT, RINSE THOROUGHLY WITH WATER.

OTC - STOP USE SECTION

STOP USE AND ASK A DOCTOR IF:

  • IRRITATION OCCURS
  • CONDITION WORSENS OR DOES NOT IMPROVE WITHIN 2 WEEKS FOR JOCK ITCH, OR WITHIN 4 WEEKS FOR ATHLETE'S FOOT AND RINGWORM.

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 IMMEDIATELY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

CLEANSE AFFECTED AREA AND DRY THOROUGHLY. APPLY A THIN LAYER TO AFFECTED AREA TWICE DAILY OR AS DIRECTED BY A PHYSICIAN.

  • FOR JOCK ITCH USE DAILY FOR TWO WEEKS.
  • FOR ATHLETE'S FOOT AND RINGWORM USE DAILY FOR FOUR WEEKS.

OTHER INFORMATION

OTHER SAFETY INFORMATION

  • THIS PRODUCT IS NOT EFFECTIVE ON THE SCALP OR NAILS.
  • STORE AT ROOM TEMPERATURE 59° - 86°F (15° - 30°C).

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

CAPRYLIC/CAPRIC TRIGLYCERIDE, CETEARETH-20, CETEARYL ALCOHOL, IMIDIAZOLIDINYL UREA, DIMETHICONE, DISODIUM EDTA, GLYCERYL STEARATE, METHYLPARABEN, PEG-40 CASTOR OIL, PEG-100 STEARATE, PETROLATUM, PROPYLENE GLYCOL, PROPYLPARABEN, STEARIC ACID, WATER, XANTHAN GUM.

QUESTIONS?

OTC - QUESTIONS SECTION

CALL 877.314.2554

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Embrace Antifungal 6oz .jpgEmbrace Antifungal 6oz .jpg

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62172-20262172-202-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML · Source PDF

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
101c3790-0b77-9612-e063-6294a90a650de267ecbc-c07c-493e-8a96-ca58a8ac8e672024-01-29WarningsExact identifier
spl set id: e267ecbc-c07c-493e-8a96-ca58a8ac8e67

Reported adverse events (FAERS/openFDA)#

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