NDC 85237-1948-01 - Pepcid Complete
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
- 85237-1948
- Requested NDC
- 85237-1948-01
- Package NDCs from labels
- 85237-1948-0, 85237-1948-1, 85237-1948-2, 85237-1948-3, 85237-1948-4, 85237-1948-01
- Manufacturer
- Select Consumer Group
- Effective date
- 2026-07-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Pepcid Complete - Select Consumer Group | Select Consumer Group | 2026-07-04 | HUMAN OTC DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| Ultra Strength Antacid | CALCIUM CARBONATE CHEWABLE TABLETS | CVS Pharmacy. Inc. | 24cec2bc-cf12-b513-e063-6394a90a9447 | 2026-06-30 | Warnings | H0G9379FGK |
| Zantac 360 | FAMOTIDINE | Select Consumer Group LLC | 529cef2d-e6cc-3b37-e063-6294a90aff59 | 2026-06-27 | Warnings | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Sportpharm LLC | 4421ceb7-a114-436c-871a-7bc5444f8154 | 2026-06-26 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Mineral oil | MINERAL OIL | CVS Pharmacy, Inc. | 1183bcbc-51ec-e53a-e063-6394a90af0f2 | 2026-06-26 | Warnings, Adverse reactions | T5L8T28FGP |
| Leukotrap RC PL System | CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM | GVS TM INC | 54eab581-bc48-f9f0-e063-6394a90a4b93 | 2026-06-25 | IY9XDZ35W2 | |
| Leukotrap WB system - CP2D | CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM | GVS TM INC | 54fdf3cf-41df-af7d-e063-6294a90ab1e6 | 2026-06-24 | IY9XDZ35W2 | |
| MILK OF MAGNESIA | MAGNESIUM HYDROXIDE | KROGER COMPANY | a1b0c638-6c34-1b72-e053-2995a90acc85 | 2026-06-24 | Warnings | NBZ3QY004S |
| Famotidine | FAMOTIDINE | RISING PHARMA HOLDINGS, INC. | c013654e-9cad-4c59-8fea-b00ae1567c18 | 2026-06-24 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | CVS Pharmacy, Inc. | 7357f67e-0fc6-4555-aa8b-1df09cba9feb | 2026-06-24 | Warnings | 5QZO15J2Z8 |
| Blood Collection System | CP2D/AS-3 TRIPLE WITH SAMPLING SYSTEM | GVS TM INC | 54e8cfd2-f91b-8381-e063-6394a90a3f77 | 2026-06-23 | IY9XDZ35W2 | |
| Leukotrap RC PL System | CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM | GVS TM INC | 54e9a497-7a94-44c9-e063-6294a90a84da | 2026-06-23 | IY9XDZ35W2 | |
| Leukotrap RC PL System | CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM | GVS TM INC | 54eb0462-cd00-4467-e063-6394a90aa371 | 2026-06-23 | IY9XDZ35W2 | |
| Leukotrap RC System | CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM | GVS TM INC | 54eb3c81-5cc8-03c4-e063-6294a90a2065 | 2026-06-23 | IY9XDZ35W2 | |
| Leukotrap RC System | CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM | GVS TM INC | 54ebb700-3bcf-d0e3-e063-6394a90a57c8 | 2026-06-23 | IY9XDZ35W2 | |
| Famotidine | FAMOTIDINE | Family Dollar Stores, LLC | 4dc7c2c4-83c7-608d-e063-6294a90a90eb | 2026-06-23 | Warnings | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Unit Dose Solutions, Inc. | 54d93bf1-8f9a-981b-e063-6394a90a0fde | 2026-06-22 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Ibuprofen Famotidine | IBUPROFEN FAMOTIDINE | Direct_Rx | 54d9e1fc-507d-1859-e063-6394a90a8c6b | 2026-06-22 | Boxed warning, Warnings, Adverse reactions | 5QZO15J2Z8 |
| Rohto Sun and Sport | HYPROMELLOSE, POVIDONE | The Mentholatum Company | 8bcc8882-b886-4b55-9bc4-d4b92a41358f | 2026-06-19 | Warnings | 3NXW29V3WO |
| Rohto Dual Light Relief | HYPROMELLOSE, POVIDONE | The Mentholatum Company | 1b597f83-d7f1-cf93-e063-6394a90a99f7 | 2026-06-19 | Warnings | 3NXW29V3WO |
| Ibuprofen and Famotidine | IBUPROFEN AND FAMOTIDINE | Advanced Rx of Tennessee, LLC | 548c705e-4094-fc6f-e063-6394a90a3426 | 2026-06-18 | Boxed warning, Warnings, Adverse reactions | 5QZO15J2Z8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.