NDC 0062-1610 - CENTANY
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
- 0062-1610
- Package NDCs from labels
- 0062-1610-01, 0062-1610-03
- Manufacturer
- OrthoNeutrogena, Division of Ortho-McNeil Pharmaceutical, Inc.
- Effective date
- 2007-02-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CENTANY ™ (mupirocin ointment),2% | OrthoNeutrogena, Division of Ortho-McNeil Pharmaceutical, Inc. | 2007-02-13 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0062-1610-01 | CENTANY | 15 g in 1 TUBE | OINTMENT | 15 | 1 | |
| 0062-1610-03 | CENTANY | 30 g in 1 TUBE | OINTMENT | 30 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| mupirocin | ACTIVE INGREDIENT | D0GX863OA5 | CENTANY (MUPIROCIN) OINTMENT [ORTHONEUTROGENA, DIVISION OF ORTHO-MCNEIL PHARMACEUTICAL, INC.] | 1 | |
| mupirocin | ACTIVE MOIETY | D0GX863OA5 | CENTANY (MUPIROCIN) OINTMENT [ORTHONEUTROGENA, DIVISION OF ORTHO-MCNEIL PHARMACEUTICAL, INC.] | 1 | |
| Castor oil | INACTIVE INGREDIENT | CENTANY (MUPIROCIN) OINTMENT [ORTHONEUTROGENA, DIVISION OF ORTHO-MCNEIL PHARMACEUTICAL, INC.] | 1 | ||
| Hard fat (Softisan 378) | INACTIVE INGREDIENT | CENTANY (MUPIROCIN) OINTMENT [ORTHONEUTROGENA, DIVISION OF ORTHO-MCNEIL PHARMACEUTICAL, INC.] | 1 | ||
| Oleyl alcohol | INACTIVE INGREDIENT | CENTANY (MUPIROCIN) OINTMENT [ORTHONEUTROGENA, DIVISION OF ORTHO-MCNEIL PHARMACEUTICAL, INC.] | 1 | ||
| Propylene glycol monostearate | INACTIVE INGREDIENT | CENTANY (MUPIROCIN) OINTMENT [ORTHONEUTROGENA, DIVISION OF ORTHO-MCNEIL PHARMACEUTICAL, INC.] | 1 |
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 |
|---|---|---|---|---|---|---|
| Mupirocin | MUPIROCIN | Advanced Rx Pharmacy of Tennessee, LLC | f1a048d9-af57-a4a2-e053-2995a90a8663 | 2024-12-31 | Warnings, Adverse reactions | 106346 |
| Mupirocin | MUPIROCIN | Advanced Rx Pharmacy of Tennessee, LLC | f1a01044-8f2e-4e91-e053-2995a90af722 | 2024-12-31 | Warnings, Adverse reactions | 106346 |
| DermacinRx Clorhexacin | MUPIROCIN OINTMENT | PureTek Corporation | 3c8cb9a6-58e5-4e8d-bfdc-1432a1bde6f9 | 2024-12-13 | Warnings, Adverse reactions | 106346 |
| Mupirocin | MUPIROCIN | NuCare Pharmaceuticals,Inc. | 66db1071-024f-aa19-e053-2a91aa0a8e39 | 2024-06-06 | Warnings, Adverse reactions | 106346 |
| mupirocin | MUPIROCIN | A-S Medication Solutions | a6c22c25-0f02-4c06-bbc2-723a18ecdda8 | 2024-01-30 | Warnings, Adverse reactions | 106346 |
| mupirocin | MUPIROCIN | Padagis Israel Pharmaceuticals Ltd | e9b61f01-3c67-42a4-a62b-10f1d1343190 | 2023-12-31 | Warnings, Adverse reactions | 106346 |
| Mupirocin | MUPIROCIN | Proficient Rx LP | 2777e4f2-2b8d-41f5-a96a-02dec8c7c3e0 | 2023-11-01 | Warnings, Adverse reactions | 106346 |
| mupirocin | MUPIROCIN | Bryant Ranch Prepack | 1cd4c71f-138b-47c2-8ce8-9ac32408dc56 | 2023-07-18 | Warnings, Adverse reactions | 106346 |
| Mupirocin | MUPIROCIN | Proficient Rx LP | d8766748-6b53-4673-a3ee-5cd8a4301647 | 2023-01-01 | Warnings, Adverse reactions | 106346 |
| Mupirocin | MUPIROCIN | Proficient Rx LP | cbb18010-f3b5-4ed7-8c03-c9203f0e360e | 2022-10-01 | Warnings, Adverse reactions | 106346 |
| Mupirocin | MUPIROCIN | Teva Pharmaceuticals USA, Inc. | a543797a-2c1c-4ea3-bd6c-227a784f92d9 | 2022-05-01 | Warnings, Adverse reactions | 106346 |
| mupirocin | MUPIROCIN | Proficient Rx LP | 97f8d67d-c422-4a26-9394-24a5ec9719d9 | 2022-04-01 | Warnings, Adverse reactions | 106346 |
| mupirocin | MUPIROCIN | Asclemed USA, Inc. | b2ff9c56-ca19-48ca-bd08-4b33edb13a08 | 2020-11-09 | Warnings, Adverse reactions | 106346 |
| 2A608591-E6B9-F6BE-9870-BFB5DFEE47ED | ae3defca-06d5-49ac-8a27-be5c4e9304d1 | 2007-02-13 | Warnings, Adverse reactions | 2A608591-E6B9-F6BE-9870-BFB5DFEE47ED ae3defca-06d5-49ac-8a27-be5c4e9304d1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.