FDA label 4d346c68-b8d9-4d5a-ae30-4df545e6800e

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 (canonical bytes are SHA-256 checked before publication)

SPL set ID
6d2cda9a-449c-4d06-8f9b-e5a2cce059fe
SPL ID
4d346c68-b8d9-4d5a-ae30-4df545e6800e
Version
6
Effective date
2010-08-23
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:30:52

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Orally and parenterally administered clindamycin has been associated with severe colitis, which may result in patient death. Use of the topical formulation of clindamycin results in absorption of the antibiotic from the skin surface. Diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported with the use of topical and systemic clindamycin. Studies indicate a toxin(s) produced by Clostridia is one primary cause of antibiotic-associated colitis. The colitis is usually characterized by severe persistent diarrhea and severe abdominal cramps and may be associated with the passage of blood and mucus. Endoscopic examination may reveal pseudomembranous colitis. Stool culture for Clostridium difficile and stool assay for C. difficile toxin may be helpful diagnostically. When significant diarrhea occurs, the drug should be discontinued. Large bowel endoscopy should be considered to establish a definitive diagnosis in cases of severe diarrhea. Antiperistaltic agents, such as opiates and diphenoxylate with atropine, may prolong and/or worsen the condition. Diarrhea, colitis, and pseudomembranous colitis have been observed to begin up to several weeks following cessation of oral and parenteral therapy with clindamycin. Mild cases of pseudomembranous colitis usually respond to drug discontinuation alone. In moderate to severe cases, consideration should be given to management with fluids and electrolytes, protein supplementation and treatment with an antibacterial drug clinically effective against C. difficile colitis. Avoid contact of Evoclin with eyes. If contact occurs, rinse eyes thoroughly with water.

Adverse reactions cross-check#

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Adverse reactions sections page 1 of 1 · 2 matching rows.

adverse reactions

ADVERSE REACTIONS The incidence of adverse events occurring in ≥1% of the patients in clinical studies comparing Evoclin and its vehicle is presented below: Selected Adverse Events Occurring in ≥1% of Subjects Adverse Event Number (%) of Subjects Evoclin Foam Vehicle Foam N = 439 N = 154 Headache 12 (3%) 1 (1%) Application site burning 27 (6%) 14 (9%) Application site pruritus 5 (1%) 5 (3%) Application site dryness 4 (1%) 5 (3%) Application site reaction, not otherwise specified 3 (1%) 4 (3%) In a contact sensitization study, none of the 203 subjects developed evidence of allergic contact sensitization to Evoclin. Orally and parenterally administered clindamycin has been associated with severe colitis, which may end fatally. Cases of diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported as adverse reactions in patients treated with oral and parenteral formulations of clindamycin and rarely with topical clindamycin (see WARNINGS ). Abdominal pain and gastrointestinal disturbances, as well as gram-negative folliculitis, have also been reported in association with the use of topical formulations of clindamycin.

adverse reactions table

<table ID="_Refid_d53b52bc-9935-4a9d-afd9-6e46eb020"> <caption>Selected Adverse Events Occurring in &#x2265;1% of Subjects</caption> <col width="47%"/> <col width="16%"/> <col width="16%"/> <tbody> <tr> <td rowspan="3" styleCode="Toprule "> <paragraph> <content styleCode="bold">Adverse Event</content> </paragraph> </td> <td align="center" colspan="2" styleCode="Toprule "> <paragraph> <content styleCode="bold">Number (%) of Subjects</content> </paragraph> </td> </tr> <tr> <td align="center"> <paragraph> <content styleCode="bold">Evoclin</content> <content styleCode="bold"> Foam</content> </paragraph> </td> <td align="center"> <paragraph> <content styleCode="bold">Vehicle Foam</content> </paragraph> </td> </tr> <tr> <td align="center"> <paragraph> <content styleCode="bold">N = 439</content> </paragraph> </td> <td align="center"> <paragraph> <content styleCode="bold">N = 154</content> </paragraph> </td> </tr> <tr> <td/> <td/> <td/> </tr> <tr> <td> <paragraph>Headache</paragraph> </td> <td align="center"> <paragraph>12 (3%)</paragraph> </td> <td align="center"> <paragraph>1 (1%)</paragraph> </td> </tr> <tr> <td> <paragraph>Application site burning</paragraph> </td> <td align="center"> <paragraph>27 (6%)</paragraph> </td> <td align="center"> <paragraph>14 (9%)</paragraph> </td> </tr> <tr> <td> <paragraph>Application site pruritus</paragraph> </td> <td align="center"> <paragraph>5 (1%)</paragraph> </td> <td align="center"> <paragraph>5 (3%)</paragraph> </td> </tr> <tr> <td> <paragraph>Application site dryness</paragraph> </td> <td align="center"> <paragraph>4 (1%)</paragraph> </td> <td align="center"> <paragraph>5 (3%)</paragraph> </td> </tr> <tr> <td styleCode="Botrule "> <paragraph>Application site reaction, not otherwise specified</paragraph> </td> <td align="center" styleCode="Botrule "> <paragraph>3 (1%)</paragraph> </td> <td align="center" styleCode="Botrule "> <paragraph>4 (3%)</paragraph> </td> </tr> </tbody> </table>

Reported adverse events (FAERS/openFDA)#

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