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 |
|---|---|---|---|---|---|---|
| IBUPROFEN AND FAMOTIDINE | IBUPROFEN AND FAMOTIDINE | Camber Pharmaceuticals, Inc. | 7dc158a2-fdfa-4a5f-8c28-0ce5650991db | 2024-07-11 | Boxed warning, Warnings, Adverse reactions | 5QZO15J2Z8 |
| Good Neighbor Pharmacy Antacid Regular Strength | CALCIUM CARBONATE | AmerisourceBergen Drug Corporation | 2847e82e-203e-4976-8c4f-4a5caa75ce00 | 2024-07-09 | Warnings | H0G9379FGK |
| Original strength heartburn prevention | FAMOTIDINE | KROGER COMPANY | ea1c2838-acbd-18e0-e053-2a95a90a3522 | 2024-07-08 | Warnings | 5QZO15J2Z8 |
| Kirkland Ultra Stregth Antacid 171AB | CALCIUM CARBONATE | COSTCO WHOLESALE COMPANY | 1bea92e8-1b94-77b0-e063-6394a90a8212 | 2024-07-08 | Warnings | H0G9379FGK |
| Famotidine | FAMOTIDINE | Contract Pharmacal Corp. | 273deac8-c2b0-423f-8662-4f16d91df216 | 2024-07-04 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Gentle Laxative | MAGNESIUM HYDROXIDE | GERI-CARE PHARMACEUTICALS, CORP | 1c462af8-af1a-391c-e063-6394a90a8b49 | 2024-07-02 | Warnings | NBZ3QY004S |
| FAMOTIDINE | FAMOTIDINE | NuCare Pharmaceuticals,Inc. | fd271deb-c748-bf26-e053-6294a90a11aa | 2024-06-28 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Regular Strength Antacid | CALCIUM CARBONATE | Amerisource Bergen | f9dd2797-c804-43c4-9d64-47de3b63a19a | 2024-06-28 | Warnings | H0G9379FGK |
| Ultra Strength Antacid Assorted Fruit | CALCIUM CARBONATE | Amerisource Bergen | d39b3a19-b0e7-409d-9e0b-ef847fe8be2f | 2024-06-26 | Warnings | H0G9379FGK |
| Extra Strength sugar free Antacid | CALCIUM CARBONATE | Amerisource Bergen | 541a8e91-9438-4ebd-8bfc-a2674f6a9c4a | 2024-06-17 | Warnings | H0G9379FGK |
| Artificial Tears | POLYVINYL ALCOHOL, POVIDONE | NuCare Pharmaceuticals,Inc. | 9c1c4911-908e-3c3c-e053-2995a90abcfc | 2024-06-14 | Warnings | FZ989GH94E |
| ANTACID AND GASRELIEF | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | GOODSENSE | a951fa64-7775-470e-e053-2995a90aefc4 | 2024-06-10 | Warnings | NBZ3QY004S |
| Famotidine | FAMOTIDINE | NuCare Pharmaceuticals,Inc. | 60cd0973-f74e-2b70-e053-2a91aa0a4361 | 2024-06-06 | Adverse reactions | 5QZO15J2Z8 |
| MINTOX MAXIMUM STRENGTH | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | NuCare Pharmaceuticals,Inc. | 5b1f4c78-d42e-32c7-e053-2991aa0a1985 | 2024-06-04 | Warnings | NBZ3QY004S |
| Famotidine | FAMOTIDINE | A-S Medication Solutions | 0abfc8e6-7fdf-4828-89f4-2202002f8489 | 2024-06-03 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | A-S Medication Solutions | 75a334ee-48b9-47e7-8225-6e595bed8a74 | 2024-06-03 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Pepcid | FAMOTIDINE | Bausch Health US LLC | a06502d9-7903-4f37-833e-e5763d502def | 2024-06-01 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Rising Pharma Holdings, Inc. | 15b87f7f-1abf-4d8a-bdbe-03bea0021a68 | 2024-05-29 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| MILK OF MAGNESIA | MAGNESIUM HYDROXIDE | WALGREEN COMPANY | 5f9cd233-6c46-5b52-e053-2991aa0ab729 | 2024-05-23 | Warnings | NBZ3QY004S |
| Gentle Laxative | MAGNESIUM HYDROXIDE | MEIJER, INC. | 11fe5bd0-585a-ad8a-e063-6294a90a3ae8 | 2024-05-22 | Warnings | NBZ3QY004S |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.