MUCUS RELIEF
- Product NDC
- 57896-794
- 11-digit product format
- 578960794
- Labeler code
- 57896
- Product ID
- 57896-794_284e3828-f883-997b-e063-6394a90ac514
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Geri-Care Pharmaceuticals, Corp
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2004-01-01
- Substance
- GUAIFENESIN
- Active strength
- 400 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 | 57896-794 | 57896-794-03 | 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… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 557ba5c1ecfa… | 9c80585c8c6e… |
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
- MUCUS RELIEF
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 400 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 495W7451VQ | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 359601 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| bb72de5d-d3c0-42fc-ae52-a3ad95214af5 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 4fe95224-f543-4dbb-9445-8cca122b48c8 | Product name | 1 | 20150609 |
| e8718272-64cb-4436-969b-176c3067c8f4 | Product name | 1 | 20150609 |
| 106ff02a-57e1-4c4c-a307-fd582ff4e311 | Product name | 1 | 20150212 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 57896-794-01 | 2021-02-15 | gc 794 |
| 57896-794-03 | 2021-02-15 | gc 794 |
| 57896-794-06 | 2021-02-15 | gc 794 |
| 57896-794-01 | 2021-01-29 | gc 794 |
| 57896-794-03 | 2021-01-29 | gc 794 |
| 57896-794-06 | 2021-01-29 | gc 794 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57896-794-01 | MUCUS RELIEF | 100 in 1 BOTTLE | TABLET | 100 | 7 | |
| 57896-794-03 | MUCUS RELIEF | 30 in 1 BOTTLE | TABLET | 30 | 7 | |
| 57896-794-06 | MUCUS RELIEF | 60 in 1 BOTTLE | TABLET | 60 | 7 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 57896-794-01 | EA - Each | 57896-794 | 381f87a8-ebdd-4389-b7c5-565cac8683b1 | 1 | 2013-08-02 |
| 57896-794-06 | EA - Each | 57896-794 | 9cd46e8c-842e-43bc-84f6-792f6156e495 | 1 | 2018-12-13 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| HISTEX-DM New Formulation | DEXTROMETHORPHAN HBR, PSEUDOEPHEDRINE HCI, AND TRIPROLIDINE HCI | Allegis Pharmaceuticals, LLC | 30010401-e5b4-2bd9-e063-6394a90a0b0b | 2025-03-10 | Warnings | M012 |
| daytime severe cold multi-symptom | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | United Natural Foods, Inc. dba UNFI | cc7c5f1c-76b7-4278-8e2a-5fbc85e022dd | 2025-03-08 | Warnings | M012 |
| Cold and Head Congestion Relief Severe | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL | WinCo Foods, LLC | a39778ba-1f63-4495-8e9b-44b0bdd7f71a | 2025-03-08 | Warnings | M012 |
| Extra Strength TYLENOL Severe Cough Plus Sore Throat Day | ACETAMINOPHEN AND DEXTROMETHORPHAN HYDROBROMIDE | Kenvue Brands LLC | 2e9540e4-bd1d-9370-e063-6294a90affcb | 2025-03-07 | Warnings | M012 |
| Herbal Cough Drops Original Herb | COUGH DROPS | Topco Associates LLC | 2fb22181-aee3-d0bf-e063-6294a90a7865 | 2025-03-06 | Warnings | M012 |
| REVASOL DAYTIME COLD AND FLU | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Rnv LLC | 2f9ddcc3-b913-f8b0-e063-6294a90a93ab | 2025-03-05 | Warnings | M012 |
| Herbal Throat Drops Lemon Mint Herb | THROAT DROPS | Topco Associates LLC | 2fa086b4-3b0e-0df8-e063-6294a90a6769 | 2025-03-05 | Warnings | M012 |
| Redicare Nasal and Sinus Decongestant | REDICARE NASAL AND SINUS DECONGESTANT | Redicare LLC | 2f24be68-f30e-d916-e063-6294a90a7e31 | 2025-03-04 | Warnings | M012 |
| Diphenhydramine HCl Oral Solution | DIPHENHYDRAMINE HCL ORAL SOLUTION | Kesin Pharma Corporation | 2f871005-de4d-8b2a-e063-6394a90aa43a | 2025-03-04 | Warnings | M012 |
| CVS Daytime Cough Relief Chews - Citrus Punch | DEXTROMETHORPHAN HBR | CVS | 2f885f1b-7ff5-251b-e063-6394a90a656f | 2025-03-04 | Warnings | M012 |
| CVS Dex-Dox Kids Nighttime Cough Suppressant | DEXTROMETHORPHAN HBR | CVS | 2f8b6f5e-399c-b033-e063-6294a90ac3d1 | 2025-03-04 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL 25 MG | Pioneer Life Sciences, LLC | ff8b096c-8f01-4a8c-a98f-e4aa4d688e95 | 2025-03-04 | Warnings | M012 |
| Menthol Cough Drops Honey Vanilla Flavor | MENTHOL | 7-ELEVEN | 2f3c43dd-175f-722e-e063-6294a90acff9 | 2025-02-28 | Warnings | M012 |
| Menthol Cough Drops Creamy Strawberry Flavor | MENTHOL AND PECTIN | 7-ELEVEN | 2f3c3c65-4178-6304-e063-6294a90a51fa | 2025-02-28 | Warnings | M012 |
| Menthol Cough Drops Creamy Strawberry Flavor | MENTHOL AND PECTIN | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | 2efbffd7-bbdd-c5f5-e063-6294a90a15f0 | 2025-02-25 | Warnings | M012 |
| Menthol Cough Drops Honey Vanilla Flavor | MENTHOL | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | 2efc46c9-a421-1998-e063-6394a90aeb64 | 2025-02-25 | Warnings | M012 |
| Redicare Cough Drops Cherry Flavored | CHERRY FLAVORED MENTHOL COUGH DROPS | Redicare LLC | 2efeaafa-ee96-37ee-e063-6394a90a9a4b | 2025-02-25 | Warnings | M012 |
| Childrens Allergy | DIPHENHYDRAMINE HCL | Genexa Inc. | e880b8d7-61c3-41cc-e053-2995a90aaaeb | 2025-02-20 | Warnings | M012 |
| Gencare-Nasal Decongestant PE | PHENYLEPHRINE HYDROCHLORIDE | Pioneer Life Sciences, LLC | 596ec923-56a0-4b6e-a69c-8d740feb75a2 | 2025-02-20 | Warnings | M012 |
| Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 2-pack | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, AND GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Kenvue Brands LLC | 77a2dc96-73ee-4ca2-b1fe-406995802606 | 2025-02-19 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 359601 | guaiFENesin 400 MG Oral Tablet | PSN | 9ed5611f-4e1d-4f71-b430-a2a949bf7fe5 | 8 |
| 359601 | guaifenesin 400 MG Oral Tablet | SCD | 9ed5611f-4e1d-4f71-b430-a2a949bf7fe5 | 8 |
| 359601 | guaiFENesin 400 MG Oral Tablet | PSN | bb72de5d-d3c0-42fc-ae52-a3ad95214af5 | 7 |
| 359601 | guaifenesin 400 MG Oral Tablet | SCD | bb72de5d-d3c0-42fc-ae52-a3ad95214af5 | 7 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 57896-794-01 | 57896079401 | 100 TABLET in 1 BOTTLE (57896-794-01) | 100 tablet | 2012-01-01 | 0000-00-00 | No | No | Current |
| 57896-794-03 | 57896079403 | 30 TABLET in 1 BOTTLE (57896-794-03) | 30 tablet | 2012-01-01 | 0000-00-00 | No | No | Current |
| 57896-794-06 | 57896079406 | 60 TABLET in 1 BOTTLE (57896-794-06) | 60 tablet | 2018-09-01 | 0000-00-00 | No | No | Current |