NDC 70710-1401-01 - CLOBETASOL PROPIONATE
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
- 70710-1401
- Requested NDC
- 70710-1401-01
- Package NDCs from labels
- 70710-1401-1, 70710-1401-2, 70710-1401-4, 70710-1401-3, 70710-1401-01
- Manufacturer
- Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited
- Effective date
- 2022-10-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CLOBETASOL - Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | 2022-10-05 | HUMAN PRESCRIPTION DRUG LABEL |
| CLOBETASOL PROPIONATE OINTMENT USP, 0.05% | Preferred Pharmaceuticals, Inc. | 2022-04-19 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1401-1 | CLOBETASOL PROPIONATE | 1 in 1 CARTON | OINTMENT | 1 | 6 | |
| 70710-1401-1 | CLOBETASOL PROPIONATE | 15 g in 1 TUBE | OINTMENT | 15 | 6 | |
| 70710-1401-2 | CLOBETASOL PROPIONATE | 1 in 1 CARTON | OINTMENT | 1 | 6 | |
| 70710-1401-2 | CLOBETASOL PROPIONATE | 30 g in 1 TUBE | OINTMENT | 30 | 6 | |
| 70710-1401-3 | CLOBETASOL PROPIONATE | 60 g in 1 TUBE | OINTMENT | 60 | 6 | |
| 70710-1401-3 | CLOBETASOL PROPIONATE | 1 in 1 CARTON | OINTMENT | 1 | 6 | |
| 70710-1401-4 | CLOBETASOL PROPIONATE | 45 g in 1 TUBE | OINTMENT | 45 | 6 | |
| 70710-1401-4 | CLOBETASOL PROPIONATE | 1 in 1 CARTON | OINTMENT | 1 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1401 | CLOBETASOL PROPIONATE OINTMENT [ZYDUS PHARMACEUTICALS USA INC.] | 6 | Current NDC, Legacy NDC, 8 package rows | 20221007_98a25409-e84e-452b-8dc5-ad87842398e1.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1401-1 | GM - Gram | 70710-1401 | dca331a7-bcc8-4f19-a9f3-51fed30ef500 | 1 | 2019-04-11 |
| 70710-1401-2 | GM - Gram | 70710-1401 | 2d156802-6d97-4fa4-82fd-eefd8cfb2731 | 1 | 2019-04-11 |
| 70710-1401-3 | GM - Gram | 70710-1401 | abe4f473-b54e-44c6-b448-6ea1d8959a62 | 1 | 2019-04-11 |
| 70710-1401-4 | GM - Gram | 70710-1401 | 8d5330df-ae86-45ca-9c89-e40f20dda0ff | 1 | 2019-04-11 |
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 | 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 |
| Advanced Healing | PETROLATUM | Family Dollar Stores, Inc | 7e64a424-afdb-4eb9-b6af-7b8123f1e207 | 2026-02-24 | Warnings, Adverse reactions | 4T6H12BN9U |
| Petroleum Skin Protectant | WHITE PETROLATUM | H E B | e6154e44-d7b2-429c-9bc7-5c064220d3fb | 2026-02-24 | Warnings, Adverse reactions | 4T6H12BN9U |
| Petroleum | WHITE PETROLATUM | H E B | ff79e42c-da3f-4aec-acf4-cc26e10a1d08 | 2026-02-24 | Warnings, Adverse reactions | 4T6H12BN9U |
| Petroleum | WHITE PETROLATUM | H E B | 460802cc-c1b9-41cb-afe3-ca4078175efb | 2026-02-24 | Warnings, Adverse reactions | 4T6H12BN9U |
| Petroleum | WHITE PETROLATUM | H E B | 2dd85211-0840-4d0d-8ba7-ea6184a50942 | 2026-02-24 | Warnings, Adverse reactions | 4T6H12BN9U |
| Petroleum | WHITE PETROLATUM | Meijer, Inc. | 12867b23-b203-4bd7-af6d-efddeead26be | 2026-02-24 | Warnings, Adverse reactions | 4T6H12BN9U |
| Pure petroleum | WHITE PETROLATUM | Better Living Brands, LLC | 75cb8f17-6ef2-403e-ab6e-d8e1e8168ec8 | 2026-02-23 | Warnings, Adverse reactions | 4T6H12BN9U |
| WHITE PETROLATUM | PETROLATUM | Sion Biotext Medical Ltd | 53ca3aeb-1d5d-4964-adb5-1cfa901642da | 2026-02-23 | Warnings | 4T6H12BN9U |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.