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 |
|---|---|---|---|---|---|---|
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | e07a064b-f680-405c-bbcd-24fac430951e | 2025-11-24 | Warnings | 059QF0KO0R |
| ULINE Eyewash | EYEWASH | Niagara Pharmaceuticals Inc. | 2d7f22d2-320b-6af1-e063-6294a90addc6 | 2025-11-24 | Warnings | 059QF0KO0R |
| Pur-Wash | EYEWASH | Niagara Pharmaceuticals, Inc. | 0d43b1c1-2699-37f1-e054-00144ff88e88 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 7289103a-5cbf-42f4-8848-e827149a43ca | 2025-11-24 | Warnings | 059QF0KO0R |
| health beyond VITAMINS AD | PETROLATUM | Nantong Health & Beyond Hygienic Products Inc. | de87da51-cf92-402c-b60f-5f28d1724124 | 2025-11-23 | Warnings | 4T6H12BN9U |
| Rain Daily Hydration and Comfort For Dry Eyes | GLYCERIN | Rain Eye Drops, LLC | 31d7c204-fb74-fb28-e063-6294a90ab330 | 2025-11-23 | Warnings | PDC6A3C0OX |
| Lights Swabsticks | ISOPROPYL ALCOHOL | Lights Medical Manufacture Co., Ltd. | 4435a4e6-46ae-f49b-e063-6394a90a1d9e | 2025-11-22 | Warnings | ND2M416302 |
| Walgreens Sport Lip Balm | AVOBENZONE, HOMOSALATE, OCTISALATE, PETROLATUM | Walgreens | e835ea72-1234-4bb3-b7e5-43051a906252 | 2025-11-21 | Warnings | 4T6H12BN9U |
| Eyewash Additive Concentrate | WATER AND PROPYLENE GLYCOL | Haws Corporation | dd168403-398c-41ff-b1df-d93e4ff39de3 | 2025-11-20 | Warnings | 059QF0KO0R |
| MK Alcohol Prep Pads Large | ISOPROPYL ALCOHOL | Changzhou Maokang Medical Products Co., Ltd | f1ff70d7-d0f2-45db-96e9-883b54c6e441 | 2025-11-20 | Warnings | ND2M416302 |
| Dukal Alcohol Prep Pad | ISOPROPYL ALCOHOL | Dukal LLC | 953b0dd6-a667-4146-815e-6845aba0309b | 2025-11-19 | Warnings | ND2M416302 |
| Dukal Sterile Alcohol Swabstick | ISOPROPYL ALCOHOL | Dukal LLC | 8e47e9ad-cea4-76a4-e053-2a95a90ae780 | 2025-11-19 | Warnings | ND2M416302 |
| Brain Liquescence | GINKGO BILOBA, COLCHICUM AUTUMNALE, CONVALLARIA MAJALIS, NUX MOSCHATA, CEREBRUM (SUIS), AGARICUS MUSCARIUS, SCUTELLARIA LATERIFLORA, ANACARDIUM ORIENTALE, RIBOFLAVINUM, AMBRA GRISEA, BARYTA CARBONICA, GLYCERINUM | Nutritional Specialties, Inc. | a5c366f3-fd42-4602-b20b-b7b15fde564e | 2025-11-19 | Warnings | PDC6A3C0OX |
| Moisture Barrier Cream | PETROLATUM, ZINC OXIDE | Derma Sciences Canada Inc. | 43e01e22-7872-8e24-e063-6394a90a17ef | 2025-11-18 | Warnings | 4T6H12BN9U |
| Hemorrhoidal Cream | GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM | Trifecta Pharmaceuticals Usa Llc | 804d7b1f-1be8-50c9-e053-2a91aa0a35d0 | 2025-11-18 | Warnings | 4T6H12BN9U PDC6A3C0OX |
| Sterile Water | WATER | Fresenius Kabi USA, LLC | fd823bef-c14c-4708-a18a-8aaa8470412f | 2025-11-18 | Warnings, Adverse reactions | 059QF0KO0R |
| Alka-Seltzer Original | ANHYDROUS CITRIC ACID, ASPIRIN, AND SODIUM BICARBONATE | R J General Corporation | dbb0d067-71f0-45e4-bc98-548cf4a90b3a | 2025-11-17 | Warnings | XF417D3PSL |
| Petroleum | WHITE PETROLATUM | QUALITY CHOICE (Chain Drug Marketing Association) | 684ac03a-f9b1-412d-8ce5-819ca132dc34 | 2025-11-17 | Warnings | 4T6H12BN9U |
| Petroleum with Cocoa | WHITE PETROLATUM | QUALITY CHOICE (Chain Drug Marketing Association) | 280d4bdb-30d3-44f2-9159-3aa9a1de9a5f | 2025-11-17 | Warnings | 4T6H12BN9U |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.