warnings
WARNINGS Ketoconazole cream, 2% is not for ophthalmic use.
Ketoconazole
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Ketoconazole
- Generic name
- KETOCONAZOLE
- Manufacturer
- Golden State Medical Supply, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 3e3cde4b-939f-4837-9920-bb6bb8416bd6
- SPL ID
- 3996f6a2-d5c7-ff54-e063-6294a90a12b7
- Version
- 4
- Effective date
- 2025-07-10
- Source export date
- 2026-10-12
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:03:30
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 075638 | derived:openfda.application_number |
| application number | ANDA075638 | openfda.application_number | |
| brand name | Ketoconazole | openfda.brand_name | |
| generic name | KETOCONAZOLE | openfda.generic_name | |
| manufacturer name | Golden State Medical Supply, Inc. | openfda.manufacturer_name | |
| ndc | package | 51407-279-60 | openfda.package_ndc |
| ndc | package | 51407-279-15 | openfda.package_ndc |
| ndc | package | 51407-279-30 | openfda.package_ndc |
| ndc | product | 51407-279 | openfda.product_ndc |
| ndc11 | package | 51407027930 | derived:openfda.package_ndc |
| ndc11 | package | 51407027915 | derived:openfda.package_ndc |
| ndc11 | package | 51407027960 | derived:openfda.package_ndc |
| rxcui | 203088 | openfda.rxcui | |
| spl id | 3996f6a2-d5c7-ff54-e063-6294a90a12b7 | id | |
| spl set id | 3e3cde4b-939f-4837-9920-bb6bb8416bd6 | set_id | |
| unii | R9400W927I | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS During clinical trials 45 (5.0%) of 905 patients treated with ketoconazole cream, 2% and 5 (2.4%) of 208 patients treated with placebo reported side effects consisting mainly of severe irritation, pruritus and stinging. One of the patients treated with ketoconazole cream developed a painful allergic reaction. In worldwide postmarketing experience, rare reports of contact dermatitis have been associated with ketoconazole cream or one of its excipients, namely propylene glycol.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.