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 |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Hikma Pharmaceuticals USA Inc. | 78ef7ad3-451d-43d0-a9b6-5cf0aadca003 | 2024-04-10 | Warnings, Adverse reactions | 059QF0KO0R |
| Sterile Water | WATER | B. Braun Medical Inc. | 8fc8d87a-3951-4ac5-97df-c161ffc90475 | 2024-04-10 | Warnings, Adverse reactions | 059QF0KO0R |
| PREPARATION H Maximum Strength | GLYCERIN, PETROLATUM, PHENYLEPHRINE HCL, PRAMOXINE HCL | Haleon US Holdings LLC | 7cc03d2e-e708-589a-d9bb-58ebbda989c0 | 2024-04-05 | Warnings | 4T6H12BN9U PDC6A3C0OX |
| ANTICOAGULANT SODIUM CITRATE | TRISODIUM CITRATE DIHYDRATE | Baxter Healthcare Corporation | 7025a0f9-1a56-4416-a3a4-925d755aed90 | 2024-04-02 | B22547B95K | |
| Isopropyl Alcohol Cleansing Pad TOALLITAS HUMEDAS CON ALCOHOL ISOPROPILICO | ISOPROPYL ALCOHOL | M-star (Hubei) Health&Care Products Co., Ltd. | 42a482ab-2a62-4c39-8ea5-5e57ef794b8f | 2024-04-01 | Warnings | ND2M416302 |
| Eye Wash | WATER | M-star (Hubei) Health&Care Products Co., Ltd. | 71706039-e250-4f08-9687-71b2928c4e46 | 2024-04-01 | Warnings | 059QF0KO0R |
| Clear Eyes Natural Tears | POLYVINYL ALCOHOL AND POVIDONE | Prestige Brands Holdings, Inc. | efba3eb0-798d-4635-b19b-4970e45b3cc9 | 2024-04-01 | Warnings | FZ989GH94E |
| ULINE Eyewash | EYEWASH | Uline. | 14545fc9-1fb4-befa-e063-6294a90a0474 | 2024-03-23 | Warnings | 059QF0KO0R |
| ChapStick Supreme Classic Cherry | WHITE PETROLATUM | Haleon US Holdings LLC | 84d8cc38-83e3-49be-b180-d01820525b60 | 2024-03-22 | Warnings | 4T6H12BN9U |
| Chapstick Moisturizer Original | AVOBENZONE, OCTINOXATE, AND WHITE PETROLATUM | Haleon US Holdings LLC | 9cd13fbb-887f-46a8-9f0b-4450ad3e07b7 | 2024-03-22 | Warnings | 4T6H12BN9U |
| Chapstick Moisturizer Cool Mint | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM | Haleon US Holdings LLC | 33497c07-ad6e-4c50-bc23-a55725b2eae1 | 2024-03-21 | Warnings | 4T6H12BN9U |
| Chapstick Moisturizer Original | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM | Haleon US Holdings LLC | de250ae9-6e4a-46ca-bcc9-5bb07dbb70c5 | 2024-03-21 | Warnings | 4T6H12BN9U |
| I.V. Prep Antiseptic Wipe | ISOPROPYL ALCOHOL | Smith & Nephew, Medical Ltd | 50f1c74a-bb8e-41c2-a7ee-f2d310a372a7 | 2024-03-21 | Warnings | ND2M416302 |
| ChapStick Classic Strawberry | WHITE PETROLATUM | Haleon US Holdings LLC | 3a279496-74c5-4ab1-ba69-06ad4a4f67cf | 2024-03-21 | Warnings | 4T6H12BN9U |
| Chapstick Moisturizer Cool Mint | AVOBENZONE, OCTINOXATE, AND WHITE PETROLATUM | Haleon US Holdings LLC | c1120c7a-1fa8-45a4-8bcf-35d9cc9f2c74 | 2024-03-21 | Warnings | 4T6H12BN9U |
| ChapStick Classic Cherry | WHITE PETROLATUM | Haleon US Holdings LLC | db041b1b-084a-4283-b6ba-4d4bcdc220b3 | 2024-03-19 | Warnings | 4T6H12BN9U |
| ChapStick Classic Original | WHITE PETROLATUM | Haleon US Holdings LLC | 42fe0f4a-efb7-4e70-a359-db7dc2ac9905 | 2024-03-19 | Warnings | 4T6H12BN9U |
| ChapStick Classic Spearmint | WHITE PETROLATUM | Haleon US Holdings LLC | 74354d8e-c265-4a27-9715-1a4c157ad890 | 2024-03-19 | Warnings | 4T6H12BN9U |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Provision Medical | ad045374-f4ad-4003-b350-8a2b0cbccb2e | 2024-03-14 | Warnings | ND2M416302 |
| REFRESH CLASSIC | POLYVINYL ALCOHOL, POVIDONE | A-S Medication Solutions | 3bf6193c-56db-45ad-844c-58eb8c33cba9 | 2024-03-14 | Warnings | FZ989GH94E |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.