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 |
|---|---|---|---|---|---|---|
| Alcohol Wipe | ISOPROPYL ALCOHOL | Walmart Inc. | 067c3983-d450-e86b-e063-6294a90ab758 | 2025-10-23 | Warnings | ND2M416302 |
| Alcohol Prep Pads | ISOPROPYL ALCOHOL | Phoenix Healthcare Solutions LLC | 24337cc6-98fe-ca0b-e063-6394a90a8b7b | 2025-10-23 | Warnings | ND2M416302 |
| Alcohol Prep Pads | ISOPROPYL ALCOHOL | PHOENIX HEALTHCARE SOLUTIONS, LLC | a225426a-c4d5-459c-bc11-2b521e08e510 | 2025-10-23 | Warnings | ND2M416302 |
| Alcohol Swabs | ISOPROPYL ALCOHOL | Phoenix Healthcare Solutions LLC | 1516d90b-4879-eb2f-e063-6294a90aa914 | 2025-10-23 | Warnings | ND2M416302 |
| Tenderphor | SKIN PROTECTANT | GERI-GENTLE CORPORATION | e6763da3-cbd1-7a86-e053-2995a90a26c1 | 2025-10-23 | Warnings | 4T6H12BN9U |
| Advanced Eye Relief Dry Eye Rejuvenation | GLYCERIN PROPYLENE GLYCOL | Bausch & Lomb Incorporated | 027969ee-64e4-4b08-bab7-c4cc8ed22f5f | 2025-10-23 | Warnings | PDC6A3C0OX |
| ChloraPrep One-Step | CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL | CareFusion 213, LLC | 8541a1ed-2a92-1fab-e053-2a91aa0a29d1 | 2025-10-23 | Warnings | ND2M416302 |
| Winco Hemorrhoidal | MINERAL OIL, PETROLATUM, AND PHENYLEPHRINE HYDROCHLORIDE | Winco Foods, LLC | 04ca3ef1-fc6b-4683-b236-a75afc031fb5 | 2025-10-23 | Warnings | 4T6H12BN9U T5L8T28FGP |
| Family Care Hemorrhoidal | MINERAL OIL | United Exchange Corp | 04375257-f4f3-48c3-a338-de43298b95eb | 2025-10-22 | Warnings | 4T6H12BN9U T5L8T28FGP |
| Family Wellness Hemorrhoidal | MINERAL OIL, PETROLATUM, AND PHENYLEPHRINE HCL | Family Dollar Services, Inc | fe3293bc-80b5-b60a-e053-6394a90a4ede | 2025-10-22 | Warnings | 4T6H12BN9U T5L8T28FGP |
| Sterile Water | WATER | Becton Dickinson and Company | cab03cda-4660-4020-a3be-bf86242ff664 | 2025-10-22 | Warnings, Adverse reactions | 059QF0KO0R |
| Refresh Relieva Preservative Free | CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN | Allergan, Inc. | 3481f9b3-5a90-40d3-80f8-81f51cc864be | 2025-10-22 | Warnings | PDC6A3C0OX |
| American Red Cross 70% Isopropyl Alcohol | ISOPROPYL ALCOHOL(70%CONC.) | Zhejiang Guoyao Jingyue Aerosol Co., Ltd. | 41b6ee3f-55f4-0502-e063-6394a90aa357 | 2025-10-21 | Warnings | ND2M416302 |
| iVIZIA Dry Eye | POVIDONE | Thea Pharma Inc. | 1ef73cb1-da48-a713-e063-6294a90afa9d | 2025-10-20 | Warnings | FZ989GH94E |
| CVS Alcohol Prep | ISOPROPYL ALCOHOL | CVS Pharmacy | 7abc66f2-faf6-421c-9c3c-b69f5a587246 | 2025-10-20 | Warnings | ND2M416302 |
| PROHEAL ALCOHOL XXL PREP PADS | ISOPROPYL ALCOHOL | Click Industries LLC | ec81be59-94a5-4675-9047-e3e82d7ad761 | 2025-10-20 | Warnings | ND2M416302 |
| ALCOHOL PREP PAD | ISOPROPYL ALCOHOL | Guangdong Comfort Medical Products Co., Ltd. | 3a2dea43-8123-3fb7-e063-6294a90a5e50 | 2025-10-19 | Warnings | ND2M416302 |
| Walgreens Antacid Pain Relief Extra Strength | ASPIRIN, CITRIC ACID, SODIUM BICARBONATE | Walgreens | b60df498-07db-500b-e053-2a95a90aff6a | 2025-10-17 | Warnings | XF417D3PSL |
| Equate Effervescent Antacid and Pain Relief | ASPIRIN, CITRIC ACID, SODIUM BICARBONATE | Walmart | 6271b34b-55a0-40a8-e053-2a91aa0acb22 | 2025-10-17 | Warnings, Adverse reactions | XF417D3PSL |
| Gerigentle-Vitamins A and D | PETROLATUM | Geri-Gentle Corporation | c36c74f7-975b-4e4c-99e3-e6921d782c71 | 2025-10-17 | Warnings | 4T6H12BN9U |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.