soothing antifungal cream

Manufacturer
Hims, Inc
Effective date
2021-01-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:49:54

Label at a glance#

Productsoothing antifungal cream
Active ingredientCLOTRIMAZOLE
Label structure12 sections

Indications and uses

Cures most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). Relieves itching, burning, cracking, scaling and discomfort which can accompany these conditions.

Dosage and administration

Wash the affected area and dry thoroughly. Apply 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 the 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,...

Label contents#

Full prescribing information#

Active Ingredient/ Purpose

OTC - ACTIVE INGREDIENT SECTION

Clotrimazole 1% w/w.................Antifungal

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • Cures most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis).
  • Relieves itching, burning, cracking, scaling and discomfort which can accompany these conditions.

Warnings

WARNINGS SECTION

Warnings

For external use only

Do not use on children under 2 years of age except under the advice of a doctor.

When using this product avoid contact with eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if

- Irritation occurs.

- There is no improvement within 4 weeks (for athlete's foot or ringworm) or within 2 weeks (for jock itch).

Keep this and all drugs out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all drugs out of the reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wash the affected area and dry thoroughly.
  • Apply 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 the 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 at controlled room temperature 15°-30° C (59°-86°F).
  • Close cap tightly after use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Dimethyl Sulfoxide, Ethylparaben, Glycerin, Glyceryl Stearate SE, Laureth-23, Light Mineral Oil, Stearyl Alcohol, Water, White Petrolatum

RECENT MAJOR CHANGES SECTION

Changed Section Header from OTC Directions to Dosage and Administration per the error message when submitting the product for validation.

Changed Section Header from OTC Uses to Indications and Usage per the error message when submitting the product for validation.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Clotrimazole 1%Clotrimazole 1%

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71730-07171730-071-01

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
bcbdf7b7-de50-465d-e053-2995a90a2cf0b3c59d23-7e18-c70c-e053-2995a90aff2d2021-03-04WarningsExact identifier
spl set id: b3c59d23-7e18-c70c-e053-2995a90aff2d

Reported adverse events (FAERS/openFDA)#

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