NDC 51672-4074-01 - 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
- 51672-4074
- Requested NDC
- 51672-4074-01
- Package NDCs from labels
- 51672-4074-5, 51672-4074-7, 51672-4074-1, 51672-4074-2, 51672-4074-6, 51672-4074-01
- 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 |
|---|---|---|---|---|---|---|
| 51672-4074-1 | Hydrocortisone Butyrate | 1 in 1 CARTON | CREAM | 1 | 5 | |
| 51672-4074-1 | Hydrocortisone Butyrate | 15 g in 1 TUBE | CREAM | 15 | 5 | |
| 51672-4074-2 | Hydrocortisone Butyrate | 30 g in 1 TUBE | CREAM | 30 | 5 | |
| 51672-4074-2 | Hydrocortisone Butyrate | 1 in 1 CARTON | CREAM | 1 | 5 | |
| 51672-4074-5 | Hydrocortisone Butyrate | 5 g in 1 TUBE | CREAM | 5 | 5 | |
| 51672-4074-6 | Hydrocortisone Butyrate | 45 g in 1 TUBE | CREAM | 45 | 5 | |
| 51672-4074-6 | Hydrocortisone Butyrate | 1 in 1 CARTON | CREAM | 1 | 5 | |
| 51672-4074-7 | Hydrocortisone Butyrate | 1 in 1 CARTON | CREAM | 1 | 5 | |
| 51672-4074-7 | Hydrocortisone Butyrate | 10 g in 1 TUBE | CREAM | 10 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-4074 | 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 |
|---|---|---|---|---|---|
| 51672-4074-1 | GM - Gram | 51672-4074 | e175c1af-8333-4d53-bdc8-9d48bb0de46f | 1 | 2012-07-24 |
| 51672-4074-6 | GM - Gram | 51672-4074 | 4eeceb59-6e4f-4111-8f59-ee88a7b420e9 | 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 |
|---|---|---|---|---|---|---|
| Fendall 2000 Pure Flow | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37dead3e-60cb-88ae-e063-6294a90a8f70 | 2026-06-24 | Warnings | 059QF0KO0R |
| Swab Applicator Brushes Iodine (0.7% Available Iodine) and Isopropyl Alcohol (74% w/w) | IODINE, ISOPROPYL ALCOHOL | XINXIANG XINDA TECHNOLOGY CO.,LTD | 54e83df5-bbeb-d068-e063-6394a90ad513 | 2026-06-23 | Warnings | ND2M416302 |
| 70% | ISOPROPYL ALCOHOL | ADUSA Distribution, LLC | f340dd7e-6412-4621-a818-2592ca78d0f2 | 2026-06-23 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | ADUSA Distribution, LLC | d95a9736-345b-4b7e-9b24-23edb3cbf7e8 | 2026-06-23 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | ADUSA Distribution, LLC | 7e066163-6629-43ad-b0b8-09c16fe94a0d | 2026-06-23 | Warnings, Adverse reactions | ND2M416302 |
| Bacteriostatic Water | BACTERIOSTATIC WATER | Fujian Genohope Biotech Ltd. | 54f66b82-c9e5-a2bc-e063-6394a90adbbc | 2026-06-23 | 059QF0KO0R | |
| Isopropyl Rubbing Alcohol 70 | ISOPROPYL ALCOHOL | Delon Laboratories (1990) Ltd. | fb481568-0c51-421f-9b73-adb4c84645aa | 2026-06-22 | Warnings | ND2M416302 |
| Medline | ISOPROPYL ALCOHOL | Medline Industries, LP | 495076e9-3187-6bfa-e063-6394a90a01f5 | 2026-06-22 | Warnings | ND2M416302 |
| Rohto Sun and Sport | HYPROMELLOSE, POVIDONE | The Mentholatum Company | 8bcc8882-b886-4b55-9bc4-d4b92a41358f | 2026-06-19 | Warnings | FZ989GH94E |
| Petroleum Skin Protectant | WHITE PETROLATUM | Walmart Inc. | e294a871-ae73-4a4f-89a3-9ebf0b4fd03a | 2026-06-19 | Warnings, Adverse reactions | 4T6H12BN9U |
| Rohto Dual Light Relief | HYPROMELLOSE, POVIDONE | The Mentholatum Company | 1b597f83-d7f1-cf93-e063-6394a90a99f7 | 2026-06-19 | Warnings | FZ989GH94E |
| Baby HealingOintment | PETROLATUM | Foshan Desha Biotechnology Co., Ltd. | 5488b81a-e5fe-1452-e063-6394a90a2ae4 | 2026-06-18 | Warnings | 4T6H12BN9U |
| Jell with Vitamin A D | LANOLIN, PETROLATUM | Jell Pharmaceuticals Pvt Ltd. | d976e5f0-1be5-d9c4-e053-2a95a90a44a4 | 2026-06-17 | Warnings | 4T6H12BN9U |
| Isopropyl alcohol 91 percent | ISOPROPYL ALCOHOL | P & L Development, LLC | fcda76cb-63c4-4e81-9e0a-13be506a8150 | 2026-06-17 | Warnings | ND2M416302 |
| Humalog | INSULIN LISPRO | Eli Lilly and Company | c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f | 2026-06-16 | Warnings, Adverse reactions | 059QF0KO0R |
| Glycerin | GLYCERIN SUPPOSITORY | Everpharm LLC | 546347e5-841e-15ca-e063-6294a90a0c8b | 2026-06-16 | Warnings | PDC6A3C0OX |
| Glycerin | GLYCERIN SUPPOSITORY | Everpharm LLC | 5463f869-2b92-4551-e063-6394a90ad6f9 | 2026-06-16 | Warnings | PDC6A3C0OX |
| MINICA-S | GLYCERIN | Sato Pharmaceutical Co., Ltd. | 687902eb-e702-4e87-a0ce-9add05e3cbc1 | 2026-06-16 | Warnings | PDC6A3C0OX |
| E-Z-GAS II | ANTACID/ANTIFLATULENT | E-Z-EM, INC. | 4e12e1cb-b033-076d-e054-00144ff8d46c | 2026-06-15 | Warnings | XF417D3PSL |
| ACD A | CITRIC ACID MONOHYDRATE, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE | Terumo BCT, Ltd. | 395aec48-198a-4aed-8e38-7accfb3232f9 | 2026-06-15 | Warnings, Adverse reactions | 2968PHW8QP B22547B95K |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.