Erythromycin and Benzoyl Peroxide
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
- Erythromycin and Benzoyl Peroxide
- Generic name
- ERYTHROMYCIN AND BENZOYL PEROXIDE
- Manufacturer
- Oceanside Pharmaceuticals
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- be5bce27-bbb7-4503-b609-d89a77ee1e05
- SPL ID
- eba108cb-67ec-4f94-8fad-0afb3a52899b
- Version
- 9
- Effective date
- 2019-06-03
- 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 05:32:22
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 | NDA | 050557 | derived:openfda.application_number |
| application number | NDA050557 | openfda.application_number | |
| brand name | Erythromycin and Benzoyl Peroxide | openfda.brand_name | |
| generic name | ERYTHROMYCIN AND BENZOYL PEROXIDE | openfda.generic_name | |
| manufacturer name | Oceanside Pharmaceuticals | openfda.manufacturer_name | |
| ndc | package | 68682-923-23 | openfda.package_ndc |
| ndc | package | 68682-925-16 | openfda.package_ndc |
| ndc | package | 68682-924-08 | openfda.package_ndc |
| ndc | package | 68682-901-46 | openfda.package_ndc |
| ndc | package | 68682-900-23 | openfda.package_ndc |
| ndc | package | 68682-922-46 | openfda.package_ndc |
| ndc | product | 68682-900 | openfda.product_ndc |
| ndc | product | 68682-901 | openfda.product_ndc |
| ndc11 | package | 68682092246 | derived:openfda.package_ndc |
| ndc11 | package | 68682090023 | derived:openfda.package_ndc |
| ndc11 | package | 68682092323 | derived:openfda.package_ndc |
| ndc11 | package | 68682092408 | derived:openfda.package_ndc |
| ndc11 | package | 68682092516 | derived:openfda.package_ndc |
| ndc11 | package | 68682090146 | derived:openfda.package_ndc |
| rxcui | 244374 | openfda.rxcui | |
| rxcui | 308694 | openfda.rxcui | |
| spl id | eba108cb-67ec-4f94-8fad-0afb3a52899b | id | |
| spl set id | be5bce27-bbb7-4503-b609-d89a77ee1e05 | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS Pseudomembranous colitis has been reported with nearly all antibacterial agents, including erythromycin, and may range in severity from mild to life-threatening. Therefore, it is important to consider this diagnosis in patients who present with diarrhea subsequent to the administration of antibacterial agents. Treatment with antibacterial agents alters the normal flora of the colon and may permit overgrowth of clostridia. Studies indicate that a toxin produced by Clostridium difficile is one primary cause of “antibiotic-associated colitis.” After the diagnosis of pseudomembranous colitis has been established, therapeutic measures should be initiated. 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.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS In controlled clinical trials, the incidence of adverse reactions associated with the use of Erythromycin-Benzoyl Peroxide Topical Gel was approximately 3%. These were dryness and urticarial reaction. The following additional local adverse reactions have been reported occasionally: irritation of the skin including peeling, itching, burning sensation, erythema, inflammation of the face, eyes and nose, and irritation of the eyes. Skin discoloration, oiliness and tenderness of the skin have also been reported. To report SUSPECTED ADVERSE REACTIONS, contact Oceanside Pharmaceuticals, at 1-800-321-4576 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.