NDC 86024-003-10 - FISH CIN
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 86024-003
- Requested NDC
- 86024-003-10
- Package NDCs from labels
- 86024-003-60, 86024-003-30, 86024-003-10
- Manufacturer
- Thomas Labs, LLC | Ohm Laboratories Inc | Chongqing Carelife Pharmaceutical Co., Ltd
- Effective date
- 2017-01-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FISH CIN | Thomas Labs, LLC | Ohm Laboratories Inc | Chongqing Carelife Pharmaceutical Co., Ltd | 2017-01-24 | OTC ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CLINDAMYCIN | ACTIVE INGREDIENT | 3U02EL437C | FISH CIN (CLINDAMYCIN) CAPSULE [THOMAS LABS, LLC] | 2 | |
| CLINDAMYCIN | ACTIVE MOIETY | 3U02EL437C | FISH CIN (CLINDAMYCIN) CAPSULE [THOMAS LABS, LLC] | 2 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Clindamycin in 5 Percent Dextrose | CLINDAMYCIN IN 5 PERCENT DEXTROSE | Civica, Inc. | 80217bd6-2bc4-401c-9345-22532b36a24f | 2026-04-24 | Boxed warning, Warnings, Adverse reactions | 3U02EL437C |
| Clindamycin in 5 Percent Dextrose | CLINDAMYCIN IN 5 PERCENT DEXTROSE | Sandoz Inc | 231d95a6-5e5f-4a45-a92b-d3d16ef0a7ca | 2026-03-02 | Boxed warning, Warnings, Adverse reactions | 3U02EL437C |
| Clindamycin in 5 percent Dextrose | CLINDAMYCIN IN PERCENT DEXTROSE | Hikma Pharmaceuticals USA Inc. | 8b452032-abed-495b-b518-15623e9850a3 | 2024-07-18 | Boxed warning, Warnings, Adverse reactions | 3U02EL437C |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.