NDC 59368-298 - injoy heartburn relief
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
- 59368-298
- Package NDCs from labels
- 59368-298-01
- Manufacturer
- Sixarp, LLC
- Effective date
- 2025-09-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| injoy heartburn relief - Sixarp, LLC | Sixarp, LLC | 2025-09-18 | HUMAN OTC DRUG LABEL |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Famotidine | FAMOTIDINE | Proficient Rx LP | 68d21d95-9603-4e68-855a-bfc65b1b58c3 | 2026-06-01 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Regular Strength Antacid Peppermint | CALCIUM CARBONATE | Hyvee Inc | 4e5526a8-d9ad-965b-e063-6294a90a8333 | 2026-06-01 | Warnings | H0G9379FGK |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Meijer Distribution Inc | 50fe57e1-6678-4697-9b35-4673db67d4fb | 2026-06-01 | Warnings | NBZ3QY004S H0G9379FGK 5QZO15J2Z8 |
| FAMOTIDINE | FAMOTIDINE | A-S Medication Solutions | e53928f3-5181-490b-acfb-be8d4cea60a9 | 2026-05-29 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| FAMOTIDINE | FAMOTIDINE | A-S Medication Solutions | 05b47b1d-f7f3-4dae-9b22-d43d2a7cfaef | 2026-05-29 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| REGULAR STRENGTH ANTACID/ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | NuCare Pharmaceuticals, Inc. | 52e75fe4-f04f-31da-e063-6294a90a1e4f | 2026-05-28 | Warnings | NBZ3QY004S |
| Ripple | GLYCERIN, POVIDONE | CorneaCare Inc | 3b5ba197-d501-681e-e063-6294a90aefb5 | 2026-05-24 | Warnings | FZ989GH94E |
| CareOne Acid Relief | FAMOTIDINE | American Sales Company | 206f5483-7de1-4bc3-af27-190e211bcb95 | 2026-05-21 | Warnings | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Bryant Ranch Prepack | cf2cd30e-9a0f-4b63-975c-5b551691cda9 | 2026-05-21 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | A-S Medication Solutions | d0558e97-3bc3-4a1e-9248-1959b0344023 | 2026-05-19 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Regular Strength Antacid Assorted Fruit Regular strength Antacid | CALCIUM CARBONATE | Hyvee Inc | 4df2a8ee-c823-7a59-e063-6394a90ac556 | 2026-05-19 | Warnings | H0G9379FGK |
| Famotidine | FAMOTIDINE | Bryant Ranch Prepack | db3af7cc-efc6-4934-acff-8bb2d31fe829 | 2026-05-19 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| good sense acid reducer | FAMOTIDINE | L. Perrigo Company | cc77f6ff-a534-4731-b971-491280840899 | 2026-05-18 | Warnings | 5QZO15J2Z8 |
| Extra Strength Antacid Assorted Fruit | CALCIUM CARBONATE | Hyvee Inc | 4cda1c1a-f5ff-5b77-e063-6294a90ad664 | 2026-05-13 | Warnings | H0G9379FGK |
| MILK OF MAGNESIA ORIGINAL | MAGNESIUM HYDROXIDE | GOODSENSE | a9509715-cc4f-595d-e053-2a95a90ae31f | 2026-05-11 | Warnings | NBZ3QY004S |
| Good Sense Acid Reducer | FAMOTIDINE | L. Perrigo Company | 39cb0f15-d177-46eb-a549-7acb885fbf07 | 2026-05-11 | Warnings | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Cardinal Health 107, LLC | 5d515c2a-dac9-42d8-aede-66d28a427dbc | 2026-05-11 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Kesin MAG-AL Plus | ALUMINUM AND MAGNESIUM HYDROXIDE W/SIMETHICONE SUSPENSION | Kesin Pharma Corporation | 436b622a-f028-df98-e063-6394a90a3eaa | 2026-05-08 | Warnings | NBZ3QY004S |
| Kesin MAG-AL Plus XS | ALUMINUM AND MAGNESIUM HYDROXIDE W/SIMETHICONE SUSPENSION | Kesin Pharma Corporation | 436b89f7-e417-0df2-e063-6394a90a96df | 2026-05-08 | Warnings | NBZ3QY004S |
| Kesin MAG-AL | ALUMINUM AND MAGNESIUM HYDROXIDE SUSPENSION | Kesin Pharma Corporation | 42df2198-14dc-da1c-e063-6394a90a1ae6 | 2026-05-08 | Warnings | NBZ3QY004S |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.