FDA label c8aeebb5-99e8-4e76-bd7f-4a141c9ee371

openFDA label record#

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SPL set ID
a53c3ef3-d89d-4c63-b3cd-521d1de531c5
SPL ID
c8aeebb5-99e8-4e76-bd7f-4a141c9ee371
Version
2
Effective date
2010-09-20
Source export date
2026-08-01
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/0689a4374f1490600b5244071db3b04bd3bbc29ceda7a856edb8225323adf20a/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:00:13

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.

Adverse reactions cross-check#

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

adverse reactions

ADVERSE REACTIONS In the one well-controlled clinical study comparing Clindagel ® and its vehicle, the incidence of skin and appendages adverse events occurring in ≥1% of the patients in either group is presented below: Number (%) of Patients Clindagel ® QD Vehicle Gel QD Body System/Adverse Event N=168 N=84 Skin and appendages disorders Dermatitis 0 (0.0) 1 (1.2) Dermatitis contact 0 (0.0) 1 (1.2) Dermatitis fungal 0 (0.0) 1 (1.2) Folliculitis 0 (0.0) 1 (1.2) Photosensitivity reaction 0 (0.0) 1 (1.2) Pruritus 1 (0.6) 1 (1.2) Rash erythematous 0 (0.0) 0 (0.0) Skin dry 0 (0.0) 0 (0.0) Peeling 1 (0.6) 0 (0.0) 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 border="0" frame="hsides"> <thead> <tr> <td align="left"> </td> <td align="center"> <content styleCode="bold">Number (%) of Patients</content> </td> <td align="center"> </td> </tr> <tr> <td align="left"> </td> <td align="center"> <content styleCode="bold">Clindagel</content> <content styleCode="bold"> <sup>&#xAE;</sup> </content> <content styleCode="bold"> QD</content> </td> <td align="center"> <content styleCode="bold">Vehicle Gel QD</content> </td> </tr> <tr> <td align="left"> <content styleCode="bold">Body System/Adverse Event</content> </td> <td align="center"> <content styleCode="bold">N=168</content> </td> <td align="center"> <content styleCode="bold">N=84</content> </td> </tr> </thead> <tbody> <tr> <td align="left">Skin and appendages disorders</td> <td align="center"/> <td align="center"/> </tr> <tr> <td align="left">Dermatitis</td> <td align="center">0 (0.0)</td> <td align="center">1 (1.2)</td> </tr> <tr> <td align="left">Dermatitis contact</td> <td align="center">0 (0.0)</td> <td align="center">1 (1.2)</td> </tr> <tr> <td align="left">Dermatitis fungal</td> <td align="center">0 (0.0)</td> <td align="center">1 (1.2)</td> </tr> <tr> <td align="left">Folliculitis</td> <td align="center">0 (0.0)</td> <td align="center">1 (1.2)</td> </tr> <tr> <td align="left">Photosensitivity reaction</td> <td align="center">0 (0.0)</td> <td align="center">1 (1.2)</td> </tr> <tr> <td align="left">Pruritus</td> <td align="center">1 (0.6)</td> <td align="center">1 (1.2)</td> </tr> <tr> <td align="left">Rash erythematous</td> <td align="center">0 (0.0)</td> <td align="center">0 (0.0)</td> </tr> <tr> <td align="left">Skin dry</td> <td align="center">0 (0.0)</td> <td align="center">0 (0.0)</td> </tr> <tr> <td align="left">Peeling</td> <td align="center">1 (0.6)</td> <td align="center">0 (0.0)</td> </tr> </tbody> </table>