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 |
|---|---|---|---|---|---|---|
| ACETAMINOPHEN AND CODEINE PHOSPHATE | ACETAMINOPHEN AND CODEINE PHOSPHATE | Bryant Ranch Prepack | 879db1b5-6365-4151-9879-80d8a2a3cd8a | 2026-03-23 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Throat Comfort Lemon Mint Ginger Drops | MENTHOL | Ricola USA Inc. | 5d7889b1-3866-49b0-97e1-1e883a52d3cb | 2026-03-23 | Warnings | M012 |
| Throat Comfort Orange Mint Cinnamon Drops | MENTHOL | Ricola USA Inc. | 1487652c-dbc1-40f4-9d59-891ec74cc363 | 2026-03-23 | Warnings | M012 |
| Mucus Relief Cold Flu and Sore Throat Maximum Strength | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | 4e2a8b53-0074-42fd-8357-a39cc6afe608 | 2026-03-23 | Warnings | M012 362O9ITL9D |
| hydrocodone bitartrate and acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Bryant Ranch Prepack | afdc6256-f7d0-404b-a377-328250ab29ff | 2026-03-23 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Mucus Relief Severe Cold Daytime Maximum Strength | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | TARGET Corporation | 5ccaf3b0-096a-4644-9c6e-9f251c167b3c | 2026-03-23 | Warnings | M012 362O9ITL9D |
| hydrocodone bitartrate and acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Bryant Ranch Prepack | 68c97e24-6898-4c17-813b-e1e62f56cb65 | 2026-03-23 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HCL | Grocery Outlet, Inc. | 4d88180f-610c-d9ab-e063-6394a90a09f0 | 2026-03-21 | Warnings | M012 362O9ITL9D |
| Cold Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE | HyVee Inc | cc371bc3-ba7a-430d-9ee4-22e9c50935f1 | 2026-03-20 | Warnings | M012 362O9ITL9D |
| hydrocodone bitartrate and acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Bryant Ranch Prepack | 2f6d0712-e756-49f2-a6b8-bbd160a454c4 | 2026-03-20 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | Mylan Institutional LLC | 1d456d07-fca2-4d43-92c0-f3b3c8b54420 | 2026-03-20 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Daytime Nighttime Multi Symptom Cold Childrens | DEXTROMETHORPHAN HBR,GUAIFENESIN,PHENYLEPHRINE HCL,ACETAMINOPHEN,DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL | Walgreens | da4c36f5-ec79-4489-bb18-8ddab79c34bd | 2026-03-20 | Warnings | M012 |
| Rapidol | ACETAMINOPHEN | Pharmadel LLC | 3a210860-1fc1-e496-e063-6394a90a8705 | 2026-03-20 | Warnings | 362O9ITL9D |
| Sanatos Daytime | ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE | Pharmadel LLC | 3bddcd5a-7776-49ff-e063-6294a90a5dd1 | 2026-03-20 | Warnings | M012 362O9ITL9D |
| Butalbital, Acetaminophen, Caffeine | BUTALBITAL, ACETAMINOPHEN, AND CAFFEINE | Preferred Pharmaceuticals Inc. | b121190e-db2a-43bb-a57d-b6683a9e2059 | 2026-03-20 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| hydrocodone bitartrate and acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Bryant Ranch Prepack | c648e299-2a8b-4530-a061-c6fd9cd1294c | 2026-03-20 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| hydrocodone bitartrate and acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Bryant Ranch Prepack | f08ea7a7-211e-4e0b-88c3-8f29a567fdc0 | 2026-03-20 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| hydrocodone bitartrate and acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Bryant Ranch Prepack | 1cdeaf5e-5f82-4820-b244-b0ec7a7307e1 | 2026-03-20 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Protect by HEALTHY SKIN LAB MD SUNSCREEN TINTED MOISTURIZER | TITANIUM DIOXIDE, ZINC OXIDE | HEALTHY SKIN LAB LIMITED | 4a1ec566-549f-45f2-a43d-dacfc7263361 | 2026-03-20 | Warnings | 15FIX9V2JP |
| Vaporizing | CAMPHOR | Amazon.com Services LLC | 21cfe9cb-5ff5-4331-8358-4d1d9646d6ac | 2026-03-19 | Warnings, Adverse reactions | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.