NDC 10631-093-35 - Kenalog
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
- 10631-093
- Requested NDC
- 10631-093-35
- Package NDCs from labels
- 10631-093-62, 10631-093-07, 10631-093-35, 10631-093-96
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | DPT Laboratories, Ltd.
- Effective date
- 2018-11-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Kenalog - Sun Pharmaceutical Industries, Inc. | DPT Laboratories, Ltd. | Sun Pharmaceutical Industries, Inc. | DPT Laboratories, Ltd. | 2018-11-09 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 10631-093-07 | GM - Gram | 10631-093 | e89eadc2-e89a-4ce6-8ad3-4dd2075a33de | 1 | 2012-07-24 |
| 10631-093-62 | GM - Gram | 10631-093 | 91a9e077-3610-4308-a5d5-ff06f9bd1a2d | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| TRIAMCINOLONE ACETONIDE | ACTIVE INGREDIENT | F446C597KA | KENALOG (TRIAMCINOLONE ACETONIDE) AEROSOL, SPRAY [RANBAXY LABORATORIES INC.] | 4 | |
| TRIAMCINOLONE ACETONIDE | ACTIVE MOIETY | F446C597KA | KENALOG (TRIAMCINOLONE ACETONIDE) AEROSOL, SPRAY [RANBAXY LABORATORIES INC.] | 4 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | KENALOG (TRIAMCINOLONE ACETONIDE) AEROSOL, SPRAY [RANBAXY LABORATORIES INC.] | 4 | |
| ISOBUTANE | INACTIVE INGREDIENT | BXR49TP611 | KENALOG (TRIAMCINOLONE ACETONIDE) AEROSOL, SPRAY [RANBAXY LABORATORIES INC.] | 4 | |
| ISOPROPYL PALMITATE | INACTIVE INGREDIENT | 8CRQ2TH63M | KENALOG (TRIAMCINOLONE ACETONIDE) AEROSOL, SPRAY [RANBAXY LABORATORIES INC.] | 4 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.