MUCUS RELIEF
- Product NDC
- 72090-044
- 11-digit product format
- 720900044
- Labeler code
- 72090
- Product ID
- 72090-044_3fcd9adf-7b5f-406c-9ab6-3460eb23fe6f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin 400 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Pioneer Life Sciences, LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-23
- 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
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 |
|---|---|
| 1695e7ea-2f83-4d3a-980e-c91be6c1f2a5 | 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 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72090-044-01 | MUCUS RELIEF | 200 in 1 BOTTLE | TABLET | 200 | 1 | |
| 72090-044-02 | MUCUS RELIEF | 300 in 1 BOTTLE | TABLET | 300 | 1 |
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 |
|---|---|---|---|---|---|---|
| Equate Menthol Chewable Gels | MENTHOL | Walmart | 1ba4b2be-7242-0a23-e063-6294a90af29c | 2025-12-23 | Warnings | M012 |
| Walgreens Severe Menthol Throat Drops | MENTHOL | Walgreens | 21dd3c68-cbc6-4799-e063-6394a90a6972 | 2025-12-23 | Warnings | M012 |
| cherry throat relief lozenges | BENZOCAINE | Zee Medical | 499d0748-538f-678c-e054-00144ff8d46c | 2025-12-23 | Warnings | M012 |
| Guaiasorb DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | NuCare Pharmaceuticals, Inc. | 46a480c7-7092-b809-e063-6294a90a60cd | 2025-12-23 | Warnings | M012 |
| menthol cough drops | MENTHOL | Winco Foods | 360a6304-206d-5475-e054-00144ff8d46c | 2025-12-23 | Warnings | M012 |
| menthol cough drops | MENTHOL | Winco Foods | 36342d8c-34ab-6178-e054-00144ff8d46c | 2025-12-23 | Warnings | M012 |
| cherry cough drops | MENTHOL | Winco Foods | 37244333-1307-5121-e054-00144ff8d46c | 2025-12-23 | Warnings | M012 |
| honey lemon cough drops | MENTHOL | Winco foods | 37718c73-880e-4a5c-e054-00144ff8d46c | 2025-12-23 | Warnings | M012 |
| honey lemon cough drops | MENTHOL | Winco Foods | 40676ddc-577f-5cc9-e054-00144ff88e88 | 2025-12-23 | Warnings | M012 |
| Sugar Free Menthol Cough Drops | MENTHOL | Winco Foods | 3788e8b6-ab9e-1513-e054-00144ff88e88 | 2025-12-23 | Warnings | M012 |
| SAFETUSSIN Non Drowsy Cough plus chest congestion | DEXTROMETHORPHAN HYDROBROMIDE, AND GUAIFENESIN | KRAMER LABORATORIES | eeca6370-29ea-4540-8139-e8461d58a286 | 2025-12-23 | Warnings | M012 |
| Tussin DM | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN | Discount Drug Mart | dd31f86b-f59e-459a-8e5f-176828706a4a | 2025-12-23 | Warnings | M012 |
| Tussin CF | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Discount Drug Mart | f8e7a08e-7422-4a1b-bfec-93e0b50d10cd | 2025-12-23 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL 25 MG | Pioneer Life Sciences, LLC | ab45ae97-7951-4058-e053-2995a90a7b2e | 2025-12-23 | Warnings | M012 |
| Childrens Chest Congestion Relief Grape | GUAIFENESIN | Discount Drug Mart | 3e5d245f-515c-4106-a855-fb97681b646a | 2025-12-23 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL 25 MG | Pioneer Life Sciences, LLC | ab45ed16-86bb-3faf-e053-2995a90acfbc | 2025-12-23 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL 25 MG | Pioneer Life Sciences, LLC | a7999da7-148a-4c6d-a2ea-0f4cc1d5b283 | 2025-12-23 | Warnings | M012 |
| Safetussin High Blood Pressure and diabetes Cough, Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND GUAIFENESIN | KRAMER LABORATORIES | 279e309c-040d-4001-808d-b7d986a9a1d8 | 2025-12-23 | Warnings | M012 |
| Sinus PE Head Congestion and Flu Severe | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 76fd1f8e-2670-421c-a9e6-c8adefb7962e | 2025-12-23 | Warnings | M012 |
| Leader Cough Drops Vanilla Honey | MENTHOL | Cardinal Health 110, LLC. DBA Leader | 1f6f1218-be7d-4b80-ad0d-eb4d1a54a1e2 | 2025-12-22 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 359601 | guaiFENesin 400 MG Oral Tablet | PSN | 1695e7ea-2f83-4d3a-980e-c91be6c1f2a5 | 1 |
| 359601 | guaiFENesin 400 MG Oral Tablet | PSN | 729ab412-f30b-4ad1-9d8f-1a5e1c48b118 | 1 |
| 359601 | guaifenesin 400 MG Oral Tablet | SCD | 1695e7ea-2f83-4d3a-980e-c91be6c1f2a5 | 1 |
| 359601 | guaifenesin 400 MG Oral Tablet | SCD | 729ab412-f30b-4ad1-9d8f-1a5e1c48b118 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 72090-044-01 | 72090004401 | 200 TABLET in 1 BOTTLE (72090-044-01) | 200 tablet | 2025-12-23 | No | No | Current |
| 72090-044-02 | 72090004402 | 300 TABLET in 1 BOTTLE (72090-044-02) | 300 tablet | 2025-04-16 | No | No | Current |