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 |
|---|---|---|---|---|---|---|
| CVS | CHILDRENS STUFFY NOSE AND COLD | CVS PHARMACY, INC | 6cff265d-94a3-4617-a366-fe970d97f05a | 2026-08-19 | Warnings | M012 04JA59TNSJ 495W7451VQ |
| CVS Severe Congestion and Pain Relief | ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | CVS | 5a8e4320-bae1-4831-b66b-9babfe8888d6 | 2026-08-19 | Warnings | M012 04JA59TNSJ 362O9ITL9D 495W7451VQ |
| CVS Mucus Relief DM Maximum Strength | DEXTROMETHORPHAN HBR AND GUAIFENESIN | CVS PHARMACY | 0ae0c244-e019-4b35-890c-8e15e3d3f7ce | 2026-08-19 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| CVS Severe Tussin CF Max | ACETAMINOPHEN, DEXTROMETHORPHAN HBR | CVS PHARMACY | e32881f5-2bb5-4756-aa86-a09473ab590b | 2026-08-19 | Warnings | M012 9D2RTI9KYH 362O9ITL9D |
| Good Sense Tussin DM Max | DEXTROMETHORPHAN HBR, GUAIFENESIN | L. Perrigo Company | d2541ef0-a73c-43aa-91ff-fdbce2748c4f | 2026-08-18 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Headache Formula Extra Strength | ACETAMINOPHEN, ASPIRIN, CAFFEINE | ARMY AND AIR FORCE EXCHANGE SERVICE | ee8d0961-7572-471f-8c96-b4c0bd354de2 | 2026-08-18 | Warnings | 362O9ITL9D |
| CVS Severe Nasal Congestion Relief Clear and Cool | OXYMETAZOLINE HYDROCHLORIDE | CVS PHARMACY, INC. | 5a7e42ee-810c-4bc1-9d8d-fac8e849e126 | 2026-08-18 | Warnings | M012 |
| DAYTIME NIGHTTIME COLD AND FLU | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Amazon.com Services LLC | 8dd039b4-209a-484a-b15e-741d55087a93 | 2026-08-18 | Warnings | M012 |
| CVS Daytime Cold and Flu Relief | ACETAMINOHPEN, DEXTROMETHORPHAN HBR, GUAIFENESIN PHENYLEPHRINE HCL | CVS PHARMACY | 558b7ed6-a9f6-452c-90cd-df8258663bf1 | 2026-08-18 | Warnings | M012 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D 495W7451VQ |
| Extra Strength Nasal | PHENYLEPHRINE HYDROCHLORIDE | CVS PHARMACY | 7acf1a9a-bd97-48bb-8025-ac26070378a2 | 2026-08-18 | Warnings | M012 04JA59TNSJ |
| Acetaminophen | ACETAMINOPHEN | Rugby Laboratories | 76f10ee2-1d6a-097c-e053-2991aa0af526 | 2026-08-18 | Warnings | 362O9ITL9D |
| Polytussin DM | DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, PYRILAMINE MALEATE | Poly Pharmaceuticals, Inc. | fda8f594-82bf-1781-e053-6294a90ad344 | 2026-08-18 | Warnings | M012 9D2RTI9KYH 04JA59TNSJ |
| Acetaminophen | ACETAMINOPHEN | Major Pharmaceuticals | 780aad35-d0f1-44b1-e053-2991aa0af9a7 | 2026-08-18 | Warnings | 362O9ITL9D |
| Mucinex Fast-Max DM Max Honey and Berry Flavor | DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN | Reckitt Benckiser LLC | da1f1ef9-a974-4998-8e1d-c1d999596943 | 2026-08-18 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Rohto Preservative Free Dry Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | f4b1974c-2412-45f6-b79d-88b8a0bcb608 | 2026-08-18 | Warnings | FZ989GH94E |
| Rohto Dry-Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | 8ea5c6c9-48f4-406a-a2cb-9280c546d87d | 2026-08-18 | Warnings | FZ989GH94E |
| CVS Health Ultra Fine Mist | OXYMETAZOLINE HYDROCHLORIDE | CVS PHARMACY, INC. | 89168715-71b1-424e-8dae-fcfa90bc85bf | 2026-08-18 | Warnings | M012 |
| CHILDRENS PAIN AND FEVER | ACETAMINOPHEN | Amazon.com Services LLC | 5eacbc4f-d20a-4c22-9680-4a648e24de43 | 2026-08-18 | Warnings | 362O9ITL9D |
| CVS Health Sinus | OXYMETAZOLINE HYDROCHLORIDE | CVS PHARMACY, INC. | c7840511-3a4f-4547-ae90-19b085a5874e | 2026-08-17 | Warnings | M012 |
| CVS Health | NASAL OXYMETAZOLINE HCL | CVS Pharmacy,Inc. | 56f08e70-bf16-4933-97bc-177bc190d12a | 2026-08-17 | Warnings | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.