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 |
|---|---|---|---|---|---|---|
| EXTRA STRENGTH PAIN RELIEVER PM | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | WALGREENS CO. | 5a58d620-a0ec-48d7-92dd-3f3f78ec10ea | 2026-01-20 | Warnings | 1092189 TC2D6JAD40 362O9ITL9D |
| Welmedix HomeCare PRO Fragile Skin Dual Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Welmedix LLC | 48da4589-0f5a-c25b-e063-6394a90ac18b | 2026-01-20 | Warnings | 15FIX9V2JP |
| KONEUK SUNSCREEN SPF50 | KONEUK SUNSCREEN SPF50 | Guangzhou Meixi Biotechnology Co., Ltd. | 48dd7f6e-2a4d-2c92-e063-6294a90a4255 | 2026-01-20 | Warnings | 15FIX9V2JP |
| Cough and Cold HBP | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR | Amerisource Bergen | 0b58990f-2246-408e-9365-51f56bb6766c | 2026-01-20 | Warnings | M012 |
| NightTime Cold and Flu Multi Symptom | ACETAMINOPHEN DEXTROMETHORPHAN HYDROBROMIDE DOXYLAMINE SUCCINATE | CARDINAL HEALTH 110, LLC. DBA LEADER 70000 | a8460fc9-2d08-4e5f-8dd3-5135ecda5923 | 2026-01-20 | Warnings | M012 362O9ITL9D |
| Leader Migraine Relief | ACETAMINOPHEN, ASPIRIN, CAFFEINE | Cardinal Health 110, LLC. dba Leader | b74a8baa-c7a2-4eed-8202-888d8ba829b9 | 2026-01-20 | Warnings | 362O9ITL9D |
| Menstrual Relief | ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE | Walgreen Company | fc258e1f-5447-421a-84a8-2d9e72fd6099 | 2026-01-20 | Warnings | 362O9ITL9D |
| Mucus Relief DM Max | DEXTROMETHORPHAN HBR, GUAIFENESIN | Family Dollar Services Inc | 0a651316-623e-41eb-ab3a-641f5d807425 | 2026-01-20 | Warnings | M012 |
| equate pain reliever | ACETAMINOPHEN | Wal-Mart Stores Inc | d4e438c6-80dd-4531-91e6-bc4ca7a8570f | 2026-01-20 | Warnings | 362O9ITL9D |
| Dior Forever Skin Glow Flawless Radiant Skin True Foundation SPF 25 2CR Cool Fosy | OCTISALATE, TITANIUM DIOXIDE | Parfums Christian Dior | 12edec55-2414-4bbd-bc96-4599a96b96ac | 2026-01-19 | Warnings | 15FIX9V2JP |
| Walgreens Maximum Strength Non Drowsy Day and Night Cold and Flu | WALGREENS MAXIMUM STRENGTH NON DROWSY DAY AND NIGHT COLD AND FLU | Walgreens | 579c47c8-6366-4785-9680-d3986ce9641d | 2026-01-19 | Warnings | M012 |
| Walgreens Maximum Strength Non-Drowsy Day and Night Sinus and Cold | WALGREENS MAXIMUM STRENGTH NON-DROWSY DAY AND NIGHT SINUS AND COLD | Walgreens | dd61c9d3-0b70-450e-9525-282710b383cc | 2026-01-19 | Warnings | M012 |
| Unishield Extra Strength Non-Aspirin | ACETAMINOPHEN | Unishield | ba0ec1eb-db85-6a7f-e053-2995a90aafe5 | 2026-01-19 | Warnings | 362O9ITL9D |
| Sinus Severe Ultra Fine Mist | OXYMETAZOLINE HYDROCHLORIDE. | VIVUNT PHARMA LLC | 48bf7422-38ef-d4b4-e063-6294a90aa3ab | 2026-01-19 | Warnings | M012 |
| OUTER REEF MINERAL SUNSCREEN SPF 30 | TITANIUM DIOXIDE | Coral Reef Park Co., Inc. | 86ee2fdf-8a88-44e6-b12a-36a92360477a | 2026-01-19 | Warnings | 15FIX9V2JP |
| Cold and Flu Daytime, Nighttime, Multi-Symptom | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Walgreens | fc670515-a820-4ea7-8786-8ae710798b31 | 2026-01-19 | Warnings | M012 |
| Allergy Relief Dye Free | DIPHENHYDRAMINE HCL | WALGREENS | 9dece7b1-00b1-2499-e053-2a95a90a0be3 | 2026-01-19 | Warnings | M012 TC2D6JAD40 |
| NIGHTTIME SLEEP AID | DIPHENHYDRAMINE HYDROCHLORIDE | WALGREEN COMPANY | f000d0b5-8ee8-4db0-99fe-aae5ed20c98e | 2026-01-19 | Warnings | TC2D6JAD40 |
| SEVERE COLD AND FLU DAYTIME NON DROWSY and NIGHTTIME | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE,GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE / ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | Walgreens | 2dba2bec-e0e3-4910-89c5-ebc093e05bec | 2026-01-19 | Warnings | M012 |
| SEVERE DAYTIME COLD and FLU DAYTIME MAXIMUM STRENGTH NON-DROWSY SEVERE | ACETAMINOPHEN, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | Walgreens | ca3c1eb4-6099-5e5f-e053-2995a90ab61b | 2026-01-19 | Warnings | M012 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.