004

Manufacturer
Shenzhen Chaoxiji Technology Co.,Ltd.
Effective date
2026-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-11 01:01:12

Label at a glance#

ProductAnti-fungal
Active ingredientCLOTRIMAZOLE
Label structure12 sections

Indications and uses

▪ Proven clinically effective in the treatment of most athlete's foot,jock itch, and ringworm. ▪ For effective relief of itching, burning, cracking, and scaling.

Dosage and administration

▪ Wash affected area well and let product sit 1-2 minutes before rinsing. ▪ Wash the affected area and dry thoroughly. ▪ Supervise children in the use of this product. ▪ For the treatment of athlete's foot: Pay special attention to the spaces between the toes,wear well-fitting and ventilated shoes, and apply once or twice daily. Change shoes and socks at least once a day. ▪ For athlete's foot and ringworm: Use dai...

Storage and handling

Store at room temperature. Avoid excessive heat and direct sunlight.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Clotrimazole 1%

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

▪ Proven clinically effective in the treatment of most athlete's foot,jock itch, and ringworm.

▪ For effective relief of itching, burning, cracking, and scaling.

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.

▪ In or near the eyes.

▪ On deep puncture wounds or serious burns.

When using this product

OTC - WHEN USING SECTION

▪ Avoid contact with the eyes.

▪ If contact occurs, rinse thoroughly with water.

▪ Stop use and ask a doctor if irritation develops or increases.

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.

▪ For the treatment of jock itch. If irritation occurs or symptoms do not improve within 2 weeks.

▪ Condition worsens or persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

▪ Keep out of reach of children.

▪ If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

▪ Wash affected area well and let product sit 1-2 minutes before rinsing.

▪ Wash the affected area and dry thoroughly.

▪ Supervise children in the use of this product.

▪ For the treatment of athlete's foot: Pay special attention to the spaces between the toes,wear well-fitting and ventilated shoes, and apply once or twice daily. Change shoes and socks at least once a day.

▪ For athlete's foot and ringworm: Use daily for 4 weeks. If the condition persists for longer than 4 weeks, consult a doctor. This product is not effective on the scalp or nails.

▪ For the treatment of jock itch: If irritation occurs or symptoms do not improve within 2 weeks, consult a doctor.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature. Avoid excessive heat and direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sucrose, Propylene Glycol, Sorbitol, Palmitic Acid, Water, Glycerin, Sodium Hydroxide, Vitamin E, Cocos Nucifera (Coconut) Oil, Aloe Barbadensis Leaf Juice, Olea Europaea (Olive) Fruit Oil, Hamamelis Virginiana (Witch Hazel) Extract, Tea Tree Oil, Ceramide NP, Cocamidopropyl Betaine, Stearic Acid, Lauric Acid, Myristic Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

87794-004-0187794-004-01

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87794-00487794-004-01

Ingredients#

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

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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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
598a5108-c89e-0bf7-e063-6394a90a87a8586d92cb-4944-0e7b-e063-6394a90a37a22026-08-21WarningsExact identifier
spl set id: 586d92cb-4944-0e7b-e063-6394a90a37a2

Reported adverse events (FAERS/openFDA)#

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