Mucinex Fast-Max
- Product NDC
- 63824-515
- 11-digit product format
- 638240515
- Labeler code
- 63824
- Product ID
- 63824-515_51b45cdb-42b6-7a6f-e063-6294a90a5039
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, Phenylephrine Hydrochloride, and Dextromethorphan Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Reckitt Benckiser LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-08-01
- Substance
- GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE
- Active strength
- 200; 5; 10 mg/1; mg/1; mg/1
- Pharmacologic classes
- Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 63824-515 | 63824-515-01 | D | Discontinued by firm | 2026-10-23 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mucinex Fast-Max
- Brand name suffix
- Severe Congestion and Cough
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 200 mg/1 |
| PHENYLEPHRINE HYDROCHLORIDE | 5 mg/1 |
| DEXTROMETHORPHAN HYDROBROMIDE | 10 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 495W7451VQ | Internal UNII lookup |
| 04JA59TNSJ | Internal UNII lookup |
| 9D2RTI9KYH | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1372652 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1991d5ee-fc90-4070-8965-cd6f4abc45cf | Available on FDA.report |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63824-515-01 | Mucinex Fast-MaxSevere Congestion and Cough | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 8 | |
| 63824-515-01 | Mucinex Fast-MaxSevere Congestion and Cough | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 8 | |
| 63824-515-20 | Mucinex Fast-MaxSevere Congestion and Cough | 5 in 1 BLISTER PACK | TABLET, FILM COATED | 5 | 8 | |
| 63824-515-20 | Mucinex Fast-MaxSevere Congestion and Cough | 4 in 1 CARTON | TABLET, FILM COATED | 4 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63824-515 | MUCINEX FAST-MAX SEVERE CONGESTION AND COUGH (GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, AND DEXTROMETHORPHAN HYDROBROMIDE) TABLET, FILM COATED [RB HEALTH (US) LLC] | 7 | Current NDC, Legacy NDC, 4 package rows | 20231202_1991d5ee-fc90-4070-8965-cd6f4abc45cf.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 |
|---|---|---|---|---|---|---|
| Mentholatum No Mess Vaporizing Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | The Mentholatum Company | f4675bc1-01cc-4a33-a3bf-bfc99230fe32 | 2024-12-17 | Warnings | M012 |
| Mentholatum Cherry Vaporizing Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | The Mentholatum Company | de01225a-eabb-4972-bf3a-3e5a0e44abef | 2024-12-17 | Warnings | M012 |
| Rite Aid Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Rite Aid Corporation | 198a666a-3f34-4e4f-89e8-ec7f412f00af | 2024-12-17 | Warnings | M012 |
| Equate Childrens Vaporizing | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Wal-Mart Stores Inc | 372e66a6-1f1f-4aa3-a2ed-d215fafee9b9 | 2024-12-17 | Warnings | M012 |
| Caring Mill Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | FSA Store Inc. | caa83419-c332-4b92-b151-22da2fa85289 | 2024-12-17 | Warnings | M012 |
| Always Save Chest Congestion Relief GUAF | GUAIFENESIN | Valu Merch | 9d81d88b-2db9-4891-942b-fecb1be961dd | 2024-12-17 | Warnings | M012 |
| Kroger EXTRA STRENGTH Acetaminophen PM Caplet | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | The Kroger Co. | 24a75ffa-c2a7-71a9-e063-6394a90a0e25 | 2024-12-17 | Warnings | M012 |
| Allergy 36ct, Caseys 4good | DIPHENHYDRAMINE HCL 25MG | Lil' Drug Store Products, Inc. | 04b78b23-424d-9762-e063-6394a90a52e3 | 2024-12-16 | Warnings | M012 |
| Sinus Relief, Caseys 4good | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL CAPLET, FILM-COATED | Lil' Drug Store Products, Inc. | 033837c0-fa68-a38d-e063-6394a90a9832 | 2024-12-16 | Warnings | M012 |
| DayQuil Severe plus VapoCOOL Cold and Flu, Travel BASIX | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Lil' Drug Store Products, Inc. | cfab9b80-0580-4482-b6e3-0aab875b5797 | 2024-12-16 | Warnings | M012 |
| Allergy Relief, 24-7 Lift by 7-Eleven | DIPHENHYDRAMINE HCL 25MG | Lil' Drug Store products, Inc. | 04c9db9a-95ef-3a48-e063-6294a90a4e8e | 2024-12-16 | Warnings | M012 |
| Cold and Flu Daytime Severe, 24/7 Life | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL TABLET | Lil' Drug Store Products, Inc. | 05cc7185-d49d-82a3-e063-6294a90a568e | 2024-12-16 | Warnings | M012 |
| Cold and Flu Nighttime Severe, 24-7 Life | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Lil' Drug Store products, Inc. | 05d0410f-164e-e7ee-e063-6394a90a2aaa | 2024-12-16 | Warnings | M012 |
| tussin dm max daytime nighttime | DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, GUAIFESESIN | CVS Pharmacy | 6feaf29e-de06-4c94-912c-a76ea2cbd8c1 | 2024-12-16 | Warnings | M012 |
| Leader Childrens Multi Symptom Cold | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | CARDINAL HEALTH 110, LLC. DBA LEADER | 169ff9cf-fcf5-46a6-b460-259421f2ec07 | 2024-12-16 | Warnings | M012 |
| Childrens Mucus and Cough Relief | DEXTROMETHORPHAN HBR, GUAIFENESIN | CARDINAL HEALTH 110, LLC. DBA LEADER | 125eeb3d-0ee2-45bb-81c0-4ca699979886 | 2024-12-16 | Warnings | M012 |
| Dextromethorphan HBr 15 mg Liquid Gels | DEXTROMETHORPHAN HBR | RUGBY LABORATORIES | cf3cc387-6642-43fd-999d-688fdaf65d4f | 2024-12-14 | Warnings | M012 |
| Allergy Relief Dye-Free Softgel | DIPHENHYDRAMINE HYDROCHLORIDE | CVS PHARMACY, INC | 60b1bb79-3ed1-438b-a27f-f7fbc108d114 | 2024-12-14 | Warnings | M012 |
| Rycontuss Cherry Flavor | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Okendpharma, Inc. | c91798fa-48ab-47a0-92da-4d44c2aafde0 | 2024-12-13 | Warnings | M012 |
| Mentholatum Lavender Vaporizing Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | The Mentholatum Company | 6f208c05-617d-492a-a016-e9d6be3c971f | 2024-12-13 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1372652 | dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet | PSN | 1991d5ee-fc90-4070-8965-cd6f4abc45cf | 8 |
| 1372652 | dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet | SCD | 1991d5ee-fc90-4070-8965-cd6f4abc45cf | 8 |
| 1372652 | dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine HCl 5 MG Oral Tablet | SY | 1991d5ee-fc90-4070-8965-cd6f4abc45cf | 8 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63824-515-01 | 63824051501 | 2 BLISTER PACK in 1 CARTON (63824-515-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 2018-08-01 | 0000-00-00 | No | No | Current |
| 63824-515-20 | 63824051520 | 4 BLISTER PACK in 1 CARTON (63824-515-20) / 5 TABLET, FILM COATED in 1 BLISTER PACK | 4 blister pack | 2024-01-01 | No | No | Current |