KetoconClear Cream

KETOCONAZOLE TOPICAL HUMAN OTC DRUG

KetoconClear Cream is an FDA drug label for the active ingredient KETOCONAZOLE manufactured by Guangzhou Shunfei Network Technology Co., Ltd. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260831.

Generic name
KETOCONAZOLE
Manufacturer
Guangzhou Shunfei Network Technology Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87976-002
Application
M005
Label effective
20260831

About this product

KetoconClear Cream is an FDA-registered drug product whose active ingredient is KETOCONAZOLE. It is labelled by Guangzhou Shunfei Network Technology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87976-002, application M005, label effective 20260831. It is one of 17 FDA drug label records sharing the active ingredient KETOCONAZOLE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing KETOCONAZOLE are most often described in connection with: treats athlete, foot jock, itch ringworm, helps relieve, itching burning, discomfort associated, fungal skin. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Ketoconazole 1%

Indications & Usage

Use Treats: • Athlete's Foot • Jock Itch • Ringworm Helps relieve itching, burning, and discomfort associated with fungal skin conditions.

Dosage & Administration

Directions Clean and dry affected area.<br>• Apply a thin layer once daily or as directed by a doctor.

Warnings

Warnings For external use only Do not use • on children under 2 years of age unless directed by a doctor When using this product • avoid contact with the eyes 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 out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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How products containing KETOCONAZOLE compare

FDA lists 17 drug label records with KETOCONAZOLE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — Guangzhou ChuanMa International Trading Co.,Ltd. 4
— — A-S Medication Solutions 3
— — Proficient Rx LP 2
— — Amerisyn LLC 1
— — Burel Pharmaceuticals, LLC 1

Frequently asked questions

What is KetoconClear Cream used for?
Use Treats: • Athlete's Foot • Jock Itch • Ringworm Helps relieve itching, burning, and discomfort associated with fungal skin conditions.

Who makes KetoconClear Cream?
Guangzhou Shunfei Network Technology Co., Ltd. is the labeler of record for KetoconClear Cream. 17 FDA label records share the active ingredient KETOCONAZOLE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does KetoconClear Cream come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is KetoconClear Cream prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing KETOCONAZOLE?
Yes. 17 FDA drug label records list KETOCONAZOLE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has KetoconClear Cream been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.