NDC 51672-4083-07 - Hydrocortisone Butyrate
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
- 51672-4083
- Requested NDC
- 51672-4083-07
- Package NDCs from labels
- 51672-4083-5, 51672-4083-7, 51672-4083-1, 51672-4083-2, 51672-4083-6, 51672-4083-07
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.
- Effective date
- 2026-07-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hydrocortisone Butyrate Ointment, 0.1% Hydrocortisone Butyrate Cream USP, 0.1% Hydrocortisone Butyrate Topical Solution, 0.1% | Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd. | 2026-07-14 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-4083-1 | Hydrocortisone Butyrate | 15 g in 1 TUBE | OINTMENT | 15 | 5 | |
| 51672-4083-1 | Hydrocortisone Butyrate | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 51672-4083-2 | Hydrocortisone Butyrate | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 51672-4083-2 | Hydrocortisone Butyrate | 30 g in 1 TUBE | OINTMENT | 30 | 5 | |
| 51672-4083-5 | Hydrocortisone Butyrate | 5 g in 1 TUBE | OINTMENT | 5 | 5 | |
| 51672-4083-6 | Hydrocortisone Butyrate | 45 g in 1 TUBE | OINTMENT | 45 | 5 | |
| 51672-4083-6 | Hydrocortisone Butyrate | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 51672-4083-7 | Hydrocortisone Butyrate | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 51672-4083-7 | Hydrocortisone Butyrate | 10 g in 1 TUBE | OINTMENT | 10 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-4083 | HYDROCORTISONE BUTYRATE SOLUTION HYDROCORTISONE BUTYRATE CREAM HYDROCORTISONE BUTYRATE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.] | 5 | Current NDC, Legacy NDC, 9 package rows | 20210409_51176835-598d-4da7-8a00-6bd36f52aa82.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-4083-1 | GM - Gram | 51672-4083 | efb8d4d9-57f2-4954-890a-9738be50e6ed | 1 | 2012-07-24 |
| 51672-4083-6 | GM - Gram | 51672-4083 | 146e42f8-c9cd-4fa2-b41a-089bcca3cb99 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| 0.25 % PHENYLEPHRINE HCl HEMORRHOIDAL | MINERAL OIL, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE | Nantong Health & Beyond Hygienic Products Inc. | 1cada0ae-3f0f-441c-a633-faa0a3009d2b | 2026-02-05 | Warnings | 4T6H12BN9U T5L8T28FGP |
| Isopropyl alcohol 50 percent | ISOPROPYL ALCOHOL | EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) | b1b52183-3296-48b2-b3d3-821c141b0bea | 2026-02-05 | Warnings | ND2M416302 |
| Isopropyl alcohol 50 percent | ISOPROPYL ALCOHOL | EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) | ee67fb96-fa2c-4542-8fdb-f2ccd885ee53 | 2026-02-05 | Warnings | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Dyad Medical Sourcing, LLC | b5c9e222-10eb-4cea-af70-213a77fcc865 | 2026-02-04 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | GoBrands, Inc. | 0fb3db50-4132-07dc-e063-6294a90a8168 | 2026-02-04 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Grocery Outlet, Inc. | 3dff8c83-7c33-7bca-e063-6394a90a675f | 2026-02-04 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl alcohol | ISOPROPYL ALCOHOL | Grocery Outlet, Inc. | 3dffba95-71c4-a2b0-e063-6394a90aaeb3 | 2026-02-04 | Warnings, Adverse reactions | ND2M416302 |
| Petroleum | WHITE PETROLATUM | Harris Teeter | de380df6-cc6e-4b2a-98de-fc08eeb6e8ea | 2026-02-04 | Warnings, Adverse reactions | 4T6H12BN9U |
| Harris Teeter | MINERAL | Harris Teeter | 401e3a7e-54be-47cc-88c3-a343f5cbbd10 | 2026-02-04 | Warnings, Adverse reactions | T5L8T28FGP |
| Petroleum | WHITE PETROLATUM | Hy-Vee, Inc. | 45867f42-9562-c111-e063-6394a90adb70 | 2026-02-04 | Warnings, Adverse reactions | 4T6H12BN9U |
| 91% ISOPROPYL ALCOHOL | 91% ISOPROPYL ALCOHOL | Hy-Vee, Inc. | 497471bb-541c-f945-e063-6294a90adbb2 | 2026-02-04 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Rubbing Alcohol | ISOPROPYL RUBBING ALCOHOL | Hy-Vee, Inc. | 4831eecf-d111-6f17-e063-6394a90a4ab9 | 2026-02-04 | Warnings, Adverse reactions | ND2M416302 |
| Petroleum Skin Protectant | WHITE PETROLATUM | Major Pharmaceuticals | 0e7e11c5-a1f8-43c4-b8a6-211491052404 | 2026-02-04 | Warnings, Adverse reactions | 4T6H12BN9U |
| Hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL | Sportpharm LLC | 88e3624d-b8bb-4e65-9250-4c51d2bbed16 | 2026-02-03 | Warnings | 4T6H12BN9U T5L8T28FGP |
| Comforts Petroleum Jelly | WHITE PETROLATUM | KROGER | 3feb3638-1cdc-62d4-e063-6294a90a1d89 | 2026-02-03 | Warnings | 4T6H12BN9U |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | CVS Pharmacy, Inc. | 5e3efd36-f11e-4e50-8936-fc54e67eebe5 | 2026-02-03 | Warnings, Adverse reactions | ND2M416302 |
| 70% | ISOPROPYL ALCOHOL | CVS Pharmacy, Inc. | fbd9086c-39b2-449c-a06d-b85ec7d2dc72 | 2026-02-03 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | CVS Pharmacy, Inc. | c5f7741b-1f11-4a34-8f11-de6975c9578d | 2026-02-03 | Warnings, Adverse reactions | ND2M416302 |
| MINIDROPS | LUBRICANT EYE DROPS | Optics Laboratory, Inc | c13c5f91-50df-471c-a7c9-1747a2ac1250 | 2026-02-03 | Warnings | FZ989GH94E |
| Vitamin A D | LANOLIN, PETROLATUM | Kroger Co. | b4aa9b58-d95e-4dac-9a34-213482e8ca34 | 2026-02-02 | Warnings, Adverse reactions | 4T6H12BN9U |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.