NDC 51672-1359-01 - Oxiconazole Nitrate
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
- 51672-1359
- Requested NDC
- 51672-1359-01
- Package NDCs from labels
- 51672-1359-1, 51672-1359-2, 51672-1359-3, 51672-1359-8, 51672-1359-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
- Effective date
- 2025-07-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CETYL ALCOHOL - Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2025-07-02 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-1359-1 | Oxiconazole Nitrate | 1 in 1 CARTON | CREAM | 1 | 7 | |
| 51672-1359-1 | Oxiconazole Nitrate | 15 g in 1 TUBE | CREAM | 15 | 7 | |
| 51672-1359-2 | Oxiconazole Nitrate | 30 g in 1 TUBE | CREAM | 30 | 7 | |
| 51672-1359-2 | Oxiconazole Nitrate | 1 in 1 CARTON | CREAM | 1 | 7 | |
| 51672-1359-3 | Oxiconazole Nitrate | 1 in 1 CARTON | CREAM | 1 | 7 | |
| 51672-1359-3 | Oxiconazole Nitrate | 60 g in 1 TUBE | CREAM | 60 | 7 | |
| 51672-1359-8 | Oxiconazole Nitrate | 1 in 1 CARTON | CREAM | 1 | 7 | |
| 51672-1359-8 | Oxiconazole Nitrate | 90 g in 1 TUBE | CREAM | 90 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-1359 | OXICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] | 6 | Current NDC, Legacy NDC, 8 package rows | 20241222_04477378-cccc-4db3-9e1b-5c1d6a00bd13.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-1359-2 | GM - Gram | 51672-1359 | a2b33705-0733-4763-97ac-069309ac7b21 | 1 | 2016-04-04 |
| 51672-1359-3 | GM - Gram | 51672-1359 | bbd47b28-7ec5-415a-9c60-8623e404a3bc | 1 | 2016-04-04 |
| 51672-1359-8 | GM - Gram | 51672-1359 | 4c9b1ca2-b80f-4fec-a067-2941c21f1723 | 1 | 2016-04-04 |
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 |
|---|---|---|---|---|---|---|
| Vitamin A D | WHITE PETROLATUM | Sion Biotext Medical Ltd. | 503c4ab9-1f60-48e2-af47-7ef996466a5b | 2026-03-09 | Warnings | 4T6H12BN9U |
| 2-Pack Facial Serum | 2-PACK FACIAL SERUM | Guangzhou Ariel Biotech Co., Ltd. | 27c7f645-cfb3-6db1-e063-6394a90a42ff | 2026-03-06 | Warnings | 059QF0KO0R |
| Advance Plus | CARDUUS MARIANUS, CYNARA SCOLYMUS, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, BENZOICUM ACIDUM, BERBERIS VULGARIS, BRYONIA (ALBA), CANTHARIS, CARDUUS BENEDICTUS, CEANOTHUS AMERICANUS, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICA, CINCHONA OFFICINALIS, DIOSCOREA VILLOSA, DOLICHOS PRURIENS, IRIS VERSICOLOR, JUNIPERUS COMMUNIS, NUX VOMICA, PTELEA TRIFOLIATA, URICUM ACIDUM | VitaminMed, LLC | 97824fb3-e2b4-4807-943b-88e26b211bf1 | 2026-03-06 | Warnings | 8SKN0B0MIM |
| Pure petroleum | WHITE PETROLATUM | Old East Main Co. | ae8583c0-1b52-461d-8506-ec7524f1b4c4 | 2026-03-02 | Warnings, Adverse reactions | 4T6H12BN9U |
| Healing for Babies | PETROLATUM | Old East Main Co. | aa1acc24-56af-4708-bf76-23d4de3d089e | 2026-03-02 | Warnings, Adverse reactions | 4T6H12BN9U |
| Petroleum | WHITE PETROLATUM | Old East Main Co. | de8d8071-ecb2-4719-8c7b-7944f27810d6 | 2026-03-02 | Warnings, Adverse reactions | 4T6H12BN9U |
| Advanced Healing | PETROLATUM | Old East Main Co. | cf916191-1de2-4305-b783-9e074c1ad94b | 2026-03-02 | Warnings, Adverse reactions | 4T6H12BN9U |
| Petroleum | WHITE PETROLATUM | The Kroger Co. | d2095c7b-61ca-40d3-bbf1-04bed4dd789c | 2026-02-27 | Warnings, Adverse reactions | 4T6H12BN9U |
| Vitamin A D | LANOLIN, PETROLATUM | Walmart Inc. | 5893801a-25e1-4750-a55b-d9cddd3f1284 | 2026-02-27 | Warnings, Adverse reactions | 4T6H12BN9U |
| Skin Protectant | PETROLATUM | Walmart Inc. | eb836922-f467-42ab-a6e7-b787d97e6c17 | 2026-02-27 | Warnings, Adverse reactions | 4T6H12BN9U |
| Advanced Healing | PETROLATUM | Walmart Inc. | aa7dbf7f-50be-475b-8140-68be3fa93507 | 2026-02-27 | Warnings, Adverse reactions | 4T6H12BN9U |
| White Petrolatum | WHITE PETROLATUM | Walmart Inc. | 176d7711-7c4f-4319-91af-0aba1260c412 | 2026-02-27 | Warnings, Adverse reactions | 4T6H12BN9U |
| Panama Jack SPF 45 Flavorless Lip Balm | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, PETROLATUM | Panama Jack | 1b15c00b-0e78-4dbe-877c-de3941ffe76e | 2026-02-26 | Warnings | 4T6H12BN9U |
| Dermatool Hemorrhoidal | GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HCL | Papalo Group LLC | 4bc06f41-7733-ebd0-e063-6294a90af7a8 | 2026-02-26 | Warnings | 4T6H12BN9U |
| Jack Black | AVOBENZONE/HOMOSALATE/OCTISALATE/PETROLATUM | Jack Black L.L.C. | 4babe2ab-c5da-9a83-e063-6294a90aee4c | 2026-02-25 | Warnings | 4T6H12BN9U |
| Jack Black | AVOBENZONE/HOMOSALATE/OCTISALATE/PETROLATUM | Jack Black L.L.C. | 4bac1c33-36fe-8d29-e063-6394a90a32a5 | 2026-02-25 | Warnings | 4T6H12BN9U |
| Jack Black | AVOBENZONE/HOMOSALATE/OCTISALATE/PETROLATUM | Jack Black L.L.C. | 4bac5550-c45f-a738-e063-6394a90ae5c8 | 2026-02-25 | Warnings | 4T6H12BN9U |
| Jack Black | AVOBENZONE/HOMOSALATE/OCTISALATE/PETROLATUM | Jack Black L.L.C. | 4baca374-7aaa-8d1d-e063-6394a90a5a55 | 2026-02-25 | Warnings | 4T6H12BN9U |
| Jack Black | AVOBENZONE/HOMOSALATE/OCTISALATE/PETROLATUM | Jack Black L.L.C. | 4bad1502-bc44-54ec-e063-6294a90ace8b | 2026-02-25 | Warnings | 4T6H12BN9U |
| Petroleum Skin Protectant | WHITE PETROLATUM | Family Dollar Stores, Inc | ac7da793-8a39-4b47-b075-a4c4820cadad | 2026-02-24 | Warnings, Adverse reactions | 4T6H12BN9U |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.