Lasolex TM AC Miconazole Nitrate 2% Antifungal Cream

Manufacturer
PureTek Corporation
Effective date
2026-06-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-06 05:10:10

Label at a glance#

ProductLasolex AC
Active ingredientMICONAZOLE NITRATE
Label structure13 sections

Indications and uses

For the treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). For relief of itching, scaling, cracking, burning, redness, soreness, irritation, discomfort, chafing associated with jock itch, itchy, scaly skin between the toes, or itching, burning feet.

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 atleast once daily. For athlete's foot and ringworm, use daily for 4 weeks,...

Storage and handling

• Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature] • Do not use if package is damaged • Protect from freezing and excessive heat • Keep container tightly closed.

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 of most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis).
  • For relief of itching, scaling, cracking, burning, redness, soreness, irritation, discomfort, chafing associated with jock itch, itchy, scaly skin between the toes, or itching, burning feet.

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 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

there is no improvement within 4 weeks (for athlete’s foot or ringworm); or there is no improvement within 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 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 atleast 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.

Other Information

STORAGE AND HANDLING SECTION

• Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature] • Do not use if package is damaged • Protect from
freezing and excessive heat • Keep container tightly closed.

Inacive ingredients

INACTIVE INGREDIENT SECTION

Aleurites moluccana (Kukui) Seed Oil, Bisabolol, Butylene Glycol, Calcium Pantothenate, Caprylyl Glycol, Carthamus tinctorius (Safflower) Oleosomes, Carthamus tinctorius (Safflower) Seed Oil, Cetyl Alcohol, Cetyl Phosphate, Chlorphenesin, Dimethyl Sulfoxide, Dimethicone, Dimethicone Crosspolymer, Disodium EDTA, dl-Alpha-Tocopheryl Acetate, Glycerin, Glyceryl Stearate, Maltodextrin, Niacinamide, PEG-100 Stearate, Pentylene Glycol, Phenoxyethanol, Pyridoxine Hydrochloride, Silica, Sodium Ascorbyl Phosphate, Sodium Hyaluronate, Sodium Hydroxide, Sodium Starch Octenylsuccinate, Stearyl Alcohol, Water, Xylitol, Zingiber officinale (Ginger) Root Extract.

For questions or information

OTC - QUESTIONS SECTION

call toll-free: 1-877-921-7873.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


Manufactured by:
PureTek Corporation
Panorama City, CA 91402


labellabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130359088239070GTIN-13: 0359088239070
EAN-13: 0359088239070
GTIN-12: 359088239070
UPC-A: 359088239070
GTIN storage (14 digits): 00359088239070
Lasolex AC.jpg

Products#

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

DailyMed product names page 1 of 1 · 36 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59088-23959088-239-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 33 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
Lasolex ACMICONAZOLE NITRATE 2% ANTIFUNGALPureTek Corporation52bb4bc1-e88f-f5ea-e063-6394a90ae1e82026-06-03WarningsExact identifier
ndc (package): 59088-239-07
ndc (product): 59088-239
ndc11 (package): 59088023907
spl id: 52bb5586-717d-f97b-e063-6294a90ac591
spl set id: 52bb4bc1-e88f-f5ea-e063-6394a90ae1e8

Reported adverse events (FAERS/openFDA)#

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