warnings
WARNINGS Clotrimazole cream is not for ophthalmic use.
Clotrimazole
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
- Clotrimazole
- Generic name
- CLOTRIMAZOLE
- Manufacturer
- Glenmark Pharmaceuticals Inc., USA
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f6898117-14f3-42d2-bc0e-d296add3ad70
- SPL ID
- 23d83b26-b5da-4474-9468-4909134295d1
- Version
- 8
- Effective date
- 2026-01-30
- Source export date
- 2026-10-12
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:45:38
| 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 | 090219 | derived:openfda.application_number |
| application number | ANDA090219 | openfda.application_number | |
| brand name | Clotrimazole | openfda.brand_name | |
| generic name | CLOTRIMAZOLE | openfda.generic_name | |
| manufacturer name | Glenmark Pharmaceuticals Inc., USA | openfda.manufacturer_name | |
| ndc | package | 68462-181-47 | openfda.package_ndc |
| ndc | package | 68462-181-17 | openfda.package_ndc |
| ndc | package | 68462-181-48 | openfda.package_ndc |
| ndc | package | 68462-181-35 | openfda.package_ndc |
| ndc | product | 68462-181 | openfda.product_ndc |
| ndc11 | package | 68462018117 | derived:openfda.package_ndc |
| ndc11 | package | 68462018147 | derived:openfda.package_ndc |
| ndc11 | package | 68462018148 | derived:openfda.package_ndc |
| ndc11 | package | 68462018135 | derived:openfda.package_ndc |
| rxcui | 309367 | openfda.rxcui | |
| spl id | 23d83b26-b5da-4474-9468-4909134295d1 | id | |
| spl set id | f6898117-14f3-42d2-bc0e-d296add3ad70 | set_id | |
| unii | G07GZ97H65 | 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 The following adverse reactions have been reported in connection with the use of this product: erythema, stinging, blistering, peeling, edema, pruritis, urticaria, burning, and general irritation of the skin.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.