NDC 79481-0149-01 - meijer EXTRA STRENGTH Pain Relief PM Caplet
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
- 79481-0149
- Requested NDC
- 79481-0149-01
- Package NDCs from labels
- 79481-0149-5, 79481-0149-1, 79481-0149-2, 79481-0149-3, 79481-0149-01
- Manufacturer
- Meijer, Inc.
- Effective date
- 2025-02-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| meijer EXTRA STRENGTH Pain Relief PM Caplet | Meijer, Inc. | 2025-02-17 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0149-1 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 100 in 1 BOTTLE | TABLET | 100 | 3 | |
| 79481-0149-1 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 1 in 1 CARTON | TABLET | 1 | 3 | |
| 79481-0149-2 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 2 in 1 CARTON | TABLET | 2 | 3 | |
| 79481-0149-2 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 100 in 1 BOTTLE | TABLET | 100 | 3 | |
| 79481-0149-3 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 1 in 1 CARTON | TABLET | 1 | 3 | |
| 79481-0149-3 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 24 in 1 BOTTLE | TABLET | 24 | 3 | |
| 79481-0149-5 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 1 in 1 CARTON | TABLET | 1 | 3 | |
| 79481-0149-5 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 50 in 1 BOTTLE | TABLET | 50 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-0149 | MEIJER EXTRA STRENGTH PAIN RELIEF PM CAPLET (ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [MEIJER, INC.] | 3 | Current NDC, 8 package rows | 20250313_1bee7e4f-1813-1bdf-e063-6294a90a6a32.zip |
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 |
|---|---|---|---|---|---|---|
| Foster and Thrive SF Honey Lemon Cough Drops | MENTHOL | McKesson | 49f41c30-f806-44ba-e063-6394a90a5a67 | 2026-02-03 | Warnings | M012 |
| Nighttime Cold and Flu Mini Softgels | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Shield Pharmaceuticals Corp | b9af8ab4-a7cb-4adf-9f6f-398c6bb7f853 | 2026-02-03 | Warnings | M012 362O9ITL9D |
| allergy relief | DIPHENHYDRAMINE HCL | Meijer Distribution Inc | 7c2fc244-bfc5-4e3c-aa90-8bc3d067b64f | 2026-02-03 | Warnings | M012 TC2D6JAD40 |
| Cold and Allergy D | PSEUDOEPHEDRINE HCL, TRIPROLIDINE HCL | Walgreen Company | 832ac849-7f4a-489a-a704-9d4388a75a71 | 2026-02-03 | Warnings | M012 |
| severe cold and flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | HyVee Inc | 987f908b-7af7-4705-bfb4-c48d771c380d | 2026-02-03 | Warnings | M012 362O9ITL9D |
| tussin dm nighttime max | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | HyVee Inc | 1f3fb451-84c9-432e-ac67-2694dd66c815 | 2026-02-03 | Warnings | M012 |
| Robafen DM Cough | DEXTROMETHORPHAN HBR, GUAIFENESIN | Major Pharmaceuticals | 7c9660b7-cb00-449b-b65f-aa42d8ce1942 | 2026-02-03 | Warnings | M012 |
| Acetaminophen | ACETAMINOPHEN | Hikma Pharmaceuticals USA Inc. | 7243bf2c-2c44-4dff-8a9e-d788d31dca86 | 2026-02-03 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Mold, Yeast and Dust | ACREMONIUM STRICTUM, ADRENALINUM, ALLIUM CEPA, ALTERNARIA ALTERNATA, ARSENICUM IODATUM, ASPERGILLUS FUMIGATUS, ASPERGILLUS NIGER, AUREOBASIDIUM PULLULANS, CANDIDA ALBICANS, CLADOSPORIUM HERBARUM, COCKROACH, DERMATOPHAGOIDES FARINAE, EPICOCCUM PURPURASCENS, FUSARIUM SOLANI, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, MUCOR CIRCINELLOIDES, NATRUM SULPHURICUM, RHIZOPUS STOLONIFER, SACCHAROMYCES CEREVISIAE, SILICEA | NaturalCare | e0f53f47-acd9-43e2-a7a2-2a500bc9dc1b | 2026-02-03 | Warnings | ETJ7Z6XBU4 |
| Allergy Relief | DIPHENHYDRAMINE HCL | Walgreen Company | 6b0d261f-fc27-4b34-88b1-cd3d72766760 | 2026-02-02 | Warnings | M012 TC2D6JAD40 |
| Hydrocodone Bitartrate and Acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | PAI Holdings, LLC dba PAI Pharma | c29b97e9-8097-4d87-a420-ccf5aec8274a | 2026-02-02 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Tussin DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | Cardinal Health 110, LLC. DBA Leader | ebfcb699-3369-4697-9841-44015b1c9808 | 2026-02-02 | Warnings | M012 |
| Dr.Oracle AIR FIT DEFENSE SOOTHING SUNSCREEN | HOMOSALATE, OCTYL SALICYLATE, TITANIUM DIOXIDE, ZINC OXIDE | Oracle Cosmetic Co., Ltd. | 21424f78-f8d5-6a9b-e063-6294a90ab7dc | 2026-02-02 | Warnings | 15FIX9V2JP |
| Cherry Sore Throat Lozenges | BENZOCAINE, MENTHOL | Meijer Distribution Inc. | 2f6de590-7cad-25d7-e054-00144ff8d46c | 2026-02-02 | Warnings | M012 |
| Mixed Berry Sore Throat and Cough lozenge | DEXTROMETHORPHAN HYDROBROMIDE | Meijer Distribution, Inc. | 304ff4db-201a-60a4-e054-00144ff8d46c | 2026-02-02 | Warnings | M012 |
| Allergy Relief Plus Congestion | DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL | Walgreen Company | 38d91107-d95c-40f2-a27e-561f951e519d | 2026-02-02 | Warnings | M012 TC2D6JAD40 |
| Menstrual Relief | ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE | DOLGENCORP, LLC | 89eb8196-54c6-4e30-8655-502cc4313c8a | 2026-02-02 | Warnings | 362O9ITL9D |
| GOODYS MAX | ACETAMINOPHEN, ASPIRIN, AND CAFFEINE | Medtech Products Inc. | 02b3a604-3f09-47e7-add1-b9038b3a268b | 2026-02-02 | Warnings | 362O9ITL9D |
| Nighttime Pain Reliever plus Sleep Aid | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | WALMART INC. | 8dd85a6b-507c-4502-9e55-a40bdf21d379 | 2026-02-02 | Warnings | TC2D6JAD40 362O9ITL9D |
| Nighttime Sleep Aid | DIPHENHYDRAMINE HCL | WinCo Foods, LLC | f446e56f-c664-4092-8712-aa3f204172f8 | 2026-02-02 | Warnings | TC2D6JAD40 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.