NDC 51672-5263-01 - Topicort
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
- 51672-5263
- Requested NDC
- 51672-5263-01
- Package NDCs from labels
- 51672-5263-5, 51672-5263-1, 51672-5263-2, 51672-5263-3, 51672-5263-7, 51672-5263-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
- Effective date
- 2026-03-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Topicort ® (Desoximetasone Ointment USP) 0.05% | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2026-03-12 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-5263-1 | Topicort | 1 in 1 CARTON | OINTMENT | 1 | 11 | |
| 51672-5263-1 | Topicort | 15 g in 1 TUBE | OINTMENT | 15 | 11 | |
| 51672-5263-2 | Topicort | 1 in 1 CARTON | OINTMENT | 1 | 11 | |
| 51672-5263-2 | Topicort | 30 g in 1 TUBE | OINTMENT | 30 | 11 | |
| 51672-5263-3 | Topicort | 1 in 1 CARTON | OINTMENT | 1 | 11 | |
| 51672-5263-3 | Topicort | 60 g in 1 TUBE | OINTMENT | 60 | 11 | |
| 51672-5263-5 | Topicort | 5 g in 1 TUBE | OINTMENT | 5 | 11 | |
| 51672-5263-5 | Topicort | 10 in 1 CARTON | OINTMENT | 10 | 11 | |
| 51672-5263-7 | Topicort | 100 g in 1 TUBE | OINTMENT | 100 | 11 | |
| 51672-5263-7 | Topicort | 1 in 1 CARTON | OINTMENT | 1 | 11 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-5263 | TOPICORT (DESOXIMETASONE) OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.] | 9 | Current NDC, Legacy NDC, 10 package rows | 20241222_96dfac6f-540f-4b7d-bcee-7e62088ebc93.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-5263-1 | GM - Gram | 51672-5263 | 06effd42-563e-4fab-a370-fa1482018d96 | 1 | 2012-07-24 |
| 51672-5263-3 | GM - Gram | 51672-5263 | 426dbc17-a78e-45d8-a8b7-fe8ee1cd646d | 1 | 2012-07-24 |
| 51672-5263-7 | GM - Gram | 51672-5263 | 634035fc-db06-4358-86b0-1a8581821516 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Desoximetasone | ACTIVE INGREDIENT | 4E07GXB7AU | TOPICORT (DESOXIMETASONE) OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.] | 7 | |
| Desoximetasone | ACTIVE MOIETY | 4E07GXB7AU | TOPICORT (DESOXIMETASONE) OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.] | 7 | |
| mineral oil | INACTIVE INGREDIENT | T5L8T28FGP | TOPICORT (DESOXIMETASONE) OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.] | 7 | |
| petrolatum | INACTIVE INGREDIENT | 4T6H12BN9U | TOPICORT (DESOXIMETASONE) OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.] | 7 |
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 |
|---|---|---|---|---|---|---|
| CVS Health Original SPF 15 Lip Balm | OXYBENZONE, OCTINOXATE, PETROLATUM | CVS | 6d58a18c-62ba-4cee-b3cc-51db746ba50e | 2016-09-14 | Warnings | 4T6H12BN9U |
| CVS Health Cherry SPF 15 Lip Balm | OXYBENZONE, OCTINOXATE, PETROLATUM | CVS | 84a621fe-890e-4c88-9f26-f013c32b52b7 | 2016-09-14 | Warnings | 4T6H12BN9U |
| CVS Health Cherry SPF 15 Lip Balm | OXYBENZONE, OCTINOXATE, PETROLATUM | CVS | bfbf0241-51a6-4d9d-bee1-741d1645037d | 2016-09-14 | Warnings | 4T6H12BN9U |
| CVS Health Original SPF 15 Lip Balm | OXYBENZONE, OCTINOXATE, PETROLATUM | CVS | e49680bd-bd61-40cf-abc8-51a1c8808726 | 2016-09-14 | Warnings | 4T6H12BN9U |
| Desoximetasone | DESOXIMETASONE | Novel Laboratories, Inc. | 781a7bba-b00d-4ceb-aefe-74c73d263b67 | 2016-06-01 | Warnings, Adverse reactions | 4E07GXB7AU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.