FDA label 8aa56680-2310-41d1-a183-4e8fb60e1415

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
3ac3fb43-39de-4e2f-a08a-1be4bf93c343
SPL ID
8aa56680-2310-41d1-a183-4e8fb60e1415
Version
2
Effective date
2011-02-11
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:48:02

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

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 pseudomembranous 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. Vancomycin has been found to be effective in the treatment of antibiotic-associated pseudomembranous colitis produced by Clostridium difficile . The usual adult dosage is 500 mg to 2 grams of vancomycin orally per day in three to four divided doses administered for 7 to 10 days. Cholestyramine or colestipol resins bind to vancomycin in vitro . If both a resin and vancomycin are to be administered concurrently, it may be advisable to separate the time of administration of each drug. Diarrhea, colitis, and pseudomembranous colitis have been observed to begin up to several weeks following cessation of oral and parenteral therapy with clindamycin.

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

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

adverse reactions

ADVERSE REACTIONS In 18 clinical studies of various formulations of clindamycin phosphate using placebo vehicle and/or active comparator drugs as controls, patients experienced a number of treatment emergent adverse dermatologic events (see table below). Number of patients reporting events Treatment Emergent Adverse Event Solution Gel Lotion n=553 (%) n=148 (%) n=160 (%) Burning 62 (11) 15 (10) 17 (11) Itching 36 (7) 15 (10) 17 (11) Burning/Itching 60 (11) # (-) # (-) Dryness 105 (19) 34 (23) 29 (18) Erythema 86 (16) 10 (7) 22 (14) Oiliness/Oily Skin 8 (1) 26 (18) 12* (10) Peeling 61 (11) # (-) 11 (7) # not recorded * of 126 subjects 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 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 width="0.000" ID="id_8816b7e2-d5f2-4ce1-a502-2d07fc68491d"> <caption ID="id_4cc43525-8eb8-4823-a9b9-d74e8888eb7d">Number of patients reporting events</caption> <col/> <col/> <col/> <col/> <tbody> <tr ID="id_17b03d40-91a5-429a-9062-55e6e269e0e1"> <td align="center" valign="middle" styleCode="Toprule">Treatment Emergent Adverse Event</td> <td align="center" valign="middle" styleCode="Toprule">Solution</td> <td align="center" valign="middle" styleCode="Toprule">Gel</td> <td align="center" valign="middle">Lotion</td> </tr> <tr ID="id_940a3dc9-6f50-4d85-819c-394e4fc885ed"> <td align="center" valign="middle"/> <td align="center" valign="middle">n=553 (%)</td> <td align="center" valign="middle">n=148 (%)</td> <td align="center" valign="middle">n=160 (%)</td> </tr> <tr ID="id_6ff5cd6c-32d6-4eb0-8b33-2caf6f7eb460"> <td align="center" valign="middle">Burning</td> <td align="center" valign="middle">62 (11)</td> <td align="center" valign="middle">15 (10)</td> <td align="center" valign="middle">17 (11)</td> </tr> <tr ID="id_1b30a313-f6b7-462b-a9c2-331e6256e5cb"> <td align="center" valign="middle">Itching</td> <td align="center" valign="middle">36 (7)</td> <td align="center" valign="middle">15 (10)</td> <td align="center" valign="middle">17 (11)</td> </tr> <tr ID="id_afef073f-1e61-43ec-b62e-c35a6d4cc152"> <td align="center" valign="middle">Burning/Itching</td> <td align="center" valign="middle">60 (11)</td> <td align="center" valign="middle"># (-)</td> <td align="center" valign="middle"># (-)</td> </tr> <tr ID="id_f3de0359-bda2-49eb-b7e9-dd34e5772d0d"> <td align="center" valign="middle">Dryness</td> <td align="center" valign="middle">105 (19)</td> <td align="center" valign="middle">34 (23)</td> <td align="center" valign="middle">29 (18)</td> </tr> <tr ID="id_2d4e58b0-cce7-407e-814e-0fa0ada5b41f"> <td align="center" valign="middle">Erythema</td> <td align="center" valign="middle">86 (16)</td> <td align="center" valign="middle">10 (7)</td> <td align="center" valign="middle">22 (14)</td> </tr> <tr ID="id_292fa209-f936-47ba-b0c3-24e8cb94f272"> <td align="center" valign="middle">Oiliness/Oily Skin</td> <td align="center" valign="middle">8 (1)</td> <td align="center" valign="middle">26 (18)</td> <td align="center" valign="middle">12* (10)</td> </tr> <tr ID="id_cce63eae-17e0-4b8c-9855-a6478f7c655f"> <td align="center" valign="middle">Peeling</td> <td align="center" valign="middle">61 (11)</td> <td align="center" valign="middle"># (-)</td> <td align="center" valign="middle">11 (7)</td> </tr> <tr ID="id_63b838fb-05e4-4979-91c9-53d1aaf073a1"> <td align="center" valign="middle"># not recorded</td> <td align="center" valign="middle"/> <td align="center" valign="middle"/> <td align="center" valign="middle"/> </tr> <tr ID="id_8d935641-052d-4bcf-9292-431f22316fef"> <td align="center" valign="middle" styleCode="Botrule">* of 126 subjects</td> <td align="center" valign="middle" styleCode="Botrule"/> <td align="center" valign="middle" styleCode="Botrule"/> <td align="center" valign="middle" styleCode="Botrule"/> </tr> </tbody> </table>

Reported adverse events (FAERS/openFDA)#

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