NDC 48951-5041-01 - Hepar Magnesium 4
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
- 48951-5041
- Requested NDC
- 48951-5041-01
- Package NDCs from labels
- 48951-5041-1, 48951-5041-01
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2025-11-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hepar Magnesium 4 | Uriel Pharmacy Inc. | 2025-11-26 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-5041-1 | Hepar Magnesium 4 | 1 mL in 1 AMPULE | LIQUID | 1 | 4 | |
| 48951-5041-1 | Hepar Magnesium 4 | 10 in 1 BOX | LIQUID | 10 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-5041 | HEPAR MAGNESIUM 4 LIQUID [URIEL PHARMACY INC.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20180522_791f416d-0cad-4526-b7c0-22042fa2de44.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| MAGNESIUM HYDROXIDE | ACTIVE INGREDIENT | NBZ3QY004S | HEPAR MAGNESIUM 4 LIQUID [URIEL PHARMACY INC.] | 1 | |
| MAMMAL LIVER | ACTIVE INGREDIENT | D0846624BI | HEPAR MAGNESIUM 4 LIQUID [URIEL PHARMACY INC.] | 1 | |
| MAGNESIUM CATION | ACTIVE MOIETY | T6V3LHY838 | HEPAR MAGNESIUM 4 LIQUID [URIEL PHARMACY INC.] | 1 | |
| MAMMAL LIVER | ACTIVE MOIETY | D0846624BI | HEPAR MAGNESIUM 4 LIQUID [URIEL PHARMACY INC.] | 1 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | HEPAR MAGNESIUM 4 LIQUID [URIEL PHARMACY INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | HEPAR MAGNESIUM 4 LIQUID [URIEL PHARMACY INC.] | 1 |
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 |
|---|---|---|---|---|---|---|
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Kenvue Brands LLC | 37e6a3f6-5261-475d-a7d4-e72854088982 | 2025-11-05 | Warnings | NBZ3QY004S |
| Dextrose in Lactated Ringers | DEXTROSE, SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE | B. Braun Medical Inc. | 190da07e-a616-46e6-b4e5-1c0ba39306e5 | 2025-11-05 | Warnings, Adverse reactions | 451W47IQ8X |
| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE | B. Braun Medical Inc. | f6d82772-638c-4584-b9d3-8833669f5963 | 2025-11-05 | Warnings, Adverse reactions | 451W47IQ8X |
| Bacteriostatic Water | BACTERIOSTATIC WATER | ProPharma Distribution | 42c6938e-f747-ae13-e063-6294a90a59a3 | 2025-11-04 | Warnings, Adverse reactions | 059QF0KO0R |
| Com-Pare2 Dual Yeast Relief Plus Multi-symptom Formula | CANDIDA ALBICANS, WOOD CREOSOTE, SODIUM CHLORIDE, SULPHUR | TRP Company | 42b6b9b9-a673-0bba-e063-6394a90a8866 | 2025-11-03 | Warnings | 451W47IQ8X |
| Potassium Chloride in Dextrose and Sodium Chloride | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, AND POTASSIUM CHLORIDE | ICU Medical Inc. | d8ee14e9-6733-4813-9f21-2b043a5f7188 | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Dextrose and Sodium Chloride | DEXTROSE MONOHYDRATE AND SODIUM CHLORIDE | ICU Medical Inc. | 4555b1bf-6d97-4798-a63d-6d34291c85ce | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Sterile Water | WATER | ICU Medical Inc. | aab10f03-26ae-4dbc-a481-ef025e48b405 | 2025-11-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Potassium Chloride in Sodium Chloride | SODIUM CHLORIDE AND POTASSIUM CHLORIDE | ICU Medical Inc. | 9dd1c001-73b3-41d4-9a96-61f6ad3a5dc3 | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Sterile Water | WATER | ICU Medical Inc. | e3484bc6-ed7f-43ef-9d49-c131a8dff2dd | 2025-11-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Sodium Chloride | SODIUM CHLORIDE | ICU Medical Inc. | 3cfdeee0-ff14-4341-8396-b11c2a037c60 | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Sodium Chloride | SODIUM CHLORIDE | ICU Medical Inc. | 5f372b75-d7a4-471e-8ac6-290040fc84b0 | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Potassium Chloride in Sodium Chloride | SODIUM CHLORIDE AND POTASSIUM CHLORIDE | ICU Medical Inc. | 243fe8fc-996a-4855-8daf-069628e547c4 | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Lactated Ringers and Dextrose | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE | ICU Medical Inc. | d310d170-5eeb-471b-af1a-0e845001d21d | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Bem Bio Antiperspirant sea breeze | MAGNESIUM HYDROXIDE,MAGNESIUM CARBONATE HYDROXIDE | Aeroflex Industria de Aerosol Ltda | 7a49fc85-c8df-46a1-ab1c-4e477bb7c2ad | 2025-10-31 | Warnings | NBZ3QY004S |
| Bem Bio Antiperspirant floral | MAGNESIUM HYDROXIDE,MAGNESIUM CARBONATE HYDROXIDE | Aeroflex Industria de Aerosol Ltda | c411f6d6-e2c2-43ff-8f4c-9b97d6268f25 | 2025-10-31 | Warnings | NBZ3QY004S |
| Bem Bio Antiperspirant original | MAGNESIUM HYDROXIDE,MAGNESIUM CARBONATE HYDROXIDE | Aeroflex Industria de Aerosol Ltda | 32dd7178-2547-4179-8d8a-ee79272aa538 | 2025-10-31 | Warnings | NBZ3QY004S |
| Bem Bio Antiperspirant unscented | MAGNESIUM HYDROXIDE,MAGNESIUM CARBONATE HYDROXIDE | Aeroflex Industria de Aerosol Ltda | 29c53638-1049-4d67-9375-00d0c3ee3348 | 2025-10-31 | Warnings | NBZ3QY004S |
| Bem Bio Antiperspirant forest trails | MAGNESIUM HYDROXIDE,MAGNESIUM CARBONATE HYDROXIDE | Aeroflex Industria de Aerosol Ltda | 412f6498-9534-4682-91fb-c8c99b559c1f | 2025-10-31 | Warnings | NBZ3QY004S |
| Family Care Saline | SODIUM CHLORIDE | United Exchange Corp. | 06737393-d4ae-3e7b-e063-6394a90ac19f | 2025-10-31 | Warnings | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.