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 |
|---|---|---|---|---|---|---|
| MUCUS AND CHEST CONGESTION | GUAIFENESIN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | f341aa99-5339-4087-a98a-469231dfc6d0 | 2026-02-17 | Warnings | 495W7451VQ |
| cold and flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | HyVee Inc | 1f3efcdd-4976-4aef-a7c6-a5f88d13cb78 | 2026-02-17 | Warnings | M012 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| MUCUS RELIEF DM | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 85ecf5bf-28a1-4b9d-9e99-c9e91ddc85e1 | 2026-02-17 | Warnings | 9D2RTI9KYH 495W7451VQ |
| Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | HyVee Inc | d5bbb5e1-ff09-4563-b2c6-149ab30e06ad | 2026-02-17 | Warnings | M012 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| Flu HBP | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR | Chain Drug Marketing Association, Inc. | 3c8f34ad-589a-4872-939c-44ad5e0e47fe | 2026-02-17 | Warnings | M012 9D2RTI9KYH 362O9ITL9D |
| CHILDRENS Acetaminophen | CHILDRENS ACETAMINOPHEN | Kesin Pharma Corporation | 4af5b025-1fd7-e825-e063-6294a90aa005 | 2026-02-16 | Warnings | 362O9ITL9D |
| Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Valu Merchandisers Company | b6144732-99da-4be2-88e0-75f31b323d38 | 2026-02-16 | Warnings, Adverse reactions | M012 |
| topcare day time cold and flu relief multi symptom relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Topco Associates LLC | 6d08ca2d-6ae4-443f-9920-34b7fb46f2b4 | 2026-02-16 | Warnings | M012 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| Infants TYLENOL | ACETAMINOPHEN | Kenvue Brands LLC | 4a121a53-dbae-05c7-e063-6294a90aed89 | 2026-02-13 | Warnings | 362O9ITL9D |
| Revasol Acetaminophen Suspension | ACETAMINOPHEN | Rnv LLC | 4ab6bb54-7c28-0c6b-e063-6394a90ac4a6 | 2026-02-13 | Warnings | M012 362O9ITL9D |
| Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Topco Associates LLC | 62eed0e8-ba5f-45c2-a543-68b50bcf4b0c | 2026-02-13 | Warnings, Adverse reactions | M012 |
| MAX relief junior Grape | CHILDRENS ACETAMINOPHEN | ATLANTIC BIOLOGICALS CORP. | 562d7901-44d6-4d9b-be8b-a8d468a22c43 | 2026-02-13 | Warnings | 362O9ITL9D |
| Revasol Acetaminophen Suspension Dye Free | ACETAMINOPHEN | Rnv LLC | 4abc07b3-6a27-260f-e063-6394a90a28d6 | 2026-02-13 | Warnings | M012 362O9ITL9D |
| robafen dm | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN | Major Pharmaceuticals | 5e19220d-9cf3-4732-b9aa-c09db5d69ce6 | 2026-02-13 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| acetaminophen | ACETAMINOPHEN | Major Pharmaceuticals | 020fa486-31f0-4e0c-84d3-5b3aaded1eeb | 2026-02-13 | Warnings | 362O9ITL9D |
| Gencare DayTime Cold and Flu Softgel | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Pioneer Life Sciences, LLC | 686b9456-f16d-4b99-ae58-f607448bed8b | 2026-02-13 | Warnings | M012 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| nasal | PHENYLEPHRINE HYDROCHLORIDE | Kroger Company | 1c3dc4e6-452b-4c84-b53c-426cf9ae8f03 | 2026-02-12 | Warnings | M012 04JA59TNSJ |
| Nighttime Cold and Flu Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE | United Natural Foods, Inc. dba UNFI | af42d3f7-661e-4322-aefe-2b7f9f1010d6 | 2026-02-12 | Warnings | M012 9D2RTI9KYH 362O9ITL9D |
| Childrens Giltuss D | CHILDRENS GILTUSS D | Gil Pharmaceutical Corp | cfc2493b-e99e-4b55-98a9-053f95d49844 | 2026-02-12 | Warnings | M012 04JA59TNSJ |
| Giltuss D | GILTUSS D | Gil Pharmaceutical Corp | 298f5457-a7df-474d-9854-68918ee3d330 | 2026-02-12 | Warnings | M012 04JA59TNSJ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.