NDC 63824-237-72 - Mucinex Fast-Max Cold, Flu and Sore Throat
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
- 63824-237
- Requested NDC
- 63824-237-72
- Package NDCs from labels
- 63824-237-20, 63824-237-72, 63824-237-44, 63824-237-21
- Manufacturer
- Reckitt Benckiser LLC
- Effective date
- 2026-05-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Mucinex Fast-Max Cold, Flu and Sore Throat - Reckitt Benckiser LLC | Reckitt Benckiser LLC | 2026-05-12 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 63824-237-20 | 2020-09-08 | Mucinex® Fast-Max ® Cold, Flu & Sore Throat |
| 63824-237-44 | 2020-09-08 | Mucinex® Fast-Max ® Cold, Flu & Sore Throat |
| 63824-237-20 | 2020-07-22 | Mucinex® Fast-Max ® Cold, Flu & Sore Throat |
| 63824-237-44 | 2020-07-22 | Mucinex® Fast-Max ® Cold, Flu & Sore Throat |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63824-237-20 | Mucinex Fast-MaxCold, Flu and Sore Throat | 2 in 1 CARTON | TABLET, COATED | 2 | 9 | |
| 63824-237-20 | Mucinex Fast-MaxCold, Flu and Sore Throat | 10 in 1 BLISTER PACK | TABLET, COATED | 10 | 9 | |
| 63824-237-21 | Mucinex Fast-MaxCold, Flu and Sore Throat | 10 in 1 BLISTER PACK | TABLET, COATED | 10 | 9 | |
| 63824-237-21 | Mucinex Fast-MaxCold, Flu and Sore Throat | 2 in 1 CARTON | TABLET, COATED | 2 | 9 | |
| 63824-237-44 | Mucinex Fast-MaxCold, Flu and Sore Throat | 4 in 1 CARTON | TABLET, COATED | 4 | 9 | |
| 63824-237-72 | Mucinex Fast-MaxCold, Flu and Sore Throat | 2 in 1 POUCH | TABLET, COATED | 2 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63824-237 | MUCINEX FAST-MAX COLD, FLU AND SORE THROAT (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [RB HEALTH (US) LLC] | 8 | Current NDC, Legacy NDC, 6 package rows | 20241222_d7c18e95-8d7b-4550-9a20-fc704a114adb.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 |
|---|---|---|---|---|---|---|
| severe cold and flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | HyVee Inc | fa8c154c-56c6-47de-8e43-9e012b4be95f | 2026-02-04 | Warnings | M012 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| Pain Relief childrens | ACETAMINOPHEN | CVS PHARMACY | b8ab85a6-3eab-4ef4-a13d-5ac300480f63 | 2026-02-03 | Warnings | 362O9ITL9D |
| Menstrual Complete | ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE | Discount Drug Mart | ba64c29d-4a50-47b7-be6b-6cf7db11a97a | 2026-02-03 | Warnings | 362O9ITL9D |
| Motrin Dual Action With Tylenol | ACETAMINOPHEN AND IBUPROFEN | Kenvue Brands LLC | f2ee9cf5-02b7-6612-e053-2995a90a90c4 | 2026-02-03 | Warnings | 362O9ITL9D |
| Hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL | Sportpharm LLC | 88e3624d-b8bb-4e65-9250-4c51d2bbed16 | 2026-02-03 | Warnings | 04JA59TNSJ |
| Foster and Thrive Cherry Cough Drops | MENTHOL | McKesson | 49eefa70-cef9-d7ec-e063-6294a90ac321 | 2026-02-03 | Warnings | M012 |
| Foster and Thrive Honey Lemon Cough Drops | MENTHOL | McKesson | 49f13ee3-6bb3-e500-e063-6394a90a152d | 2026-02-03 | Warnings | M012 |
| Daytime Cold and Flu Mini Softgels | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Shield Pharmaceuticals Corp | 63cb19d4-2306-4723-a95e-9d2d8b9eccd0 | 2026-02-03 | Warnings | M012 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| MINIDROPS | LUBRICANT EYE DROPS | Optics Laboratory, Inc | c13c5f91-50df-471c-a7c9-1747a2ac1250 | 2026-02-03 | Warnings | 532B59J990 FZ989GH94E |
| 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 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| allergy relief | DIPHENHYDRAMINE HCL | Meijer Distribution Inc | 7c2fc244-bfc5-4e3c-aa90-8bc3d067b64f | 2026-02-03 | Warnings | M012 |
| 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 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D 495W7451VQ |
| tussin dm nighttime max | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | HyVee Inc | 1f3fb451-84c9-432e-ac67-2694dd66c815 | 2026-02-03 | Warnings | M012 9D2RTI9KYH |
| Robafen DM Cough | DEXTROMETHORPHAN HBR, GUAIFENESIN | Major Pharmaceuticals | 7c9660b7-cb00-449b-b65f-aa42d8ce1942 | 2026-02-03 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Acetaminophen | ACETAMINOPHEN | Hikma Pharmaceuticals USA Inc. | 7243bf2c-2c44-4dff-8a9e-d788d31dca86 | 2026-02-03 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| mucus er | GUAIFENESIN | HyVee Inc | 74136552-55b2-4dee-9c66-3f84e9dc63d6 | 2026-02-03 | Warnings | 495W7451VQ |
| Allergy Relief | DIPHENHYDRAMINE HCL | Walgreen Company | 6b0d261f-fc27-4b34-88b1-cd3d72766760 | 2026-02-02 | Warnings | M012 |
| 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 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.