Ciclopirox
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
- Ciclopirox
- Generic name
- CICLOPIROX
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b44b190b-8e2a-4937-a6c5-92f37911e7f8
- SPL ID
- 39620da3-e63e-e94f-e063-6294a90afd69
- Version
- 8
- Effective date
- 2025-07-07
- Source export date
- 2026-09-28
- 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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:45:52
| 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 | 090269 | derived:openfda.application_number |
| application number | ANDA090269 | openfda.application_number | |
| brand name | Ciclopirox | openfda.brand_name | |
| generic name | CICLOPIROX | openfda.generic_name | |
| manufacturer name | Sun Pharmaceutical Industries, Inc. | openfda.manufacturer_name | |
| ndc | package | 51672-1351-8 | openfda.package_ndc |
| ndc | product | 51672-1351 | openfda.product_ndc |
| ndc11 | package | 51672135108 | derived:openfda.package_ndc |
| spl id | 39620da3-e63e-e94f-e063-6294a90afd69 | id | |
| spl set id | b44b190b-8e2a-4937-a6c5-92f37911e7f8 | set_id | |
| unii | 19W019ZDRJ | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5 WARNINGS AND PRECAUTIONS If signs of irritation occur, discontinue use. ( 5.1 ) Avoid contact with eyes. ( 5.1 ) Hair discoloration has been reported with Ciclopirox use. ( 5.1 ) 5.1 Local Effects If a reaction suggesting sensitivity or irritation occurs with the use of Ciclopirox Shampoo 1%, treatment should be discontinued and appropriate therapy instituted. Contact of Ciclopirox Shampoo 1% with the eyes should be avoided. If contact occurs, rinse thoroughly with water. In patients with lighter hair color, hair discoloration has been reported.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6 ADVERSE REACTIONS The most frequently reported adverse reactions are pruritus, burning, and erythema. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Taro at 1-866-923-4914 or FDA at 1-800-FDA-1088 or http://www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice. In 626 subjects treated with Ciclopirox Shampoo 1% twice weekly in the two pivotal clinical trials, the most frequent adverse events were increased itching in 1% of subjects, and application site reactions, such as burning, erythema, and itching, also in 1% of subjects. 6.2 Post Marketing Experience The following adverse reactions have been identified during post approval use of Ciclopirox Shampoo 1%: hair discoloration and abnormal hair texture, alopecia, irritation and rash. Because these events are reported voluntarily from a population of uncertain size, it is not possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.