Guaifenesin
- Product NDC
- 58657-509
- 11-digit product format
- 586570509
- Labeler code
- 58657
- Product ID
- 58657-509_41b52068-d18f-5c54-e063-6394a90aa503
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Method Pharmaceuticals, LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-02-09
- Substance
- GUAIFENESIN
- Active strength
- 100 mg/5mL
- 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
- Guaifenesin
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 100 mg/5mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 495W7451VQ | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 310604 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 312ce620-4841-7488-e054-00144ff88e88 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 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 |
| 6084a4f4-5437-c9a5-caec-5361ee075a59 | Product name | 1 | 20140508 |
| 90c5639a-61b0-88d6-ddcf-21888e94869a | Product name | 1 | 20140508 |
| 9514609b-a2a9-f8ec-6ba6-3f8e5ee89877 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 58657-509-16 | Guaifenesin | 473 mL in 1 BOTTLE | LIQUID | 473 | 9 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 58657-509-16 | ML - Milliliter | 58657-509 | 3ae23965-f0cf-41d6-95fe-ed03df86f2e1 | 1 | 2016-06-14 |
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 |
|---|---|---|---|---|---|---|
| topcare childrens cold cough | BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE | Topco Associates LLC | 40a6a7e3-6ec9-4005-9406-9d5b044b3c21 | 2025-06-16 | Warnings | M012 |
| Daytime Nighttime Sinus Relief | ACETAMINOPHEN, DIPHENHYDRAMINE HCL, GUAIFENESIN, PHENYLEPHRINE HCL | Target Corporation | 23f50b88-52c3-2029-e063-6394a90ac73e | 2025-06-14 | Warnings | M012 |
| Cough Drops Dollar General Berries Flavor 25ct | PECTIN | Dollar General Corporation | c53c19a9-5984-4b08-ae46-a53dc8bb7d74 | 2025-06-13 | Warnings | M012 |
| Cough Drops Dollar General Strawberry Flavor 25ct | PECTIN | Dollar General Corporation | d82034ca-b7fd-48c8-ab4a-8e1e56418324 | 2025-06-13 | Warnings | M012 |
| Diphenhydramine HCL | DIPHENHYDRAMINE HCL | Belleview Biosciences | 1db57d86-39f0-f8ca-e063-6394a90a6397 | 2025-06-12 | Warnings | M012 |
| TARGET Cold and Cough and Nighttime Value Pack | BROMPHENIRAMINE MALEATE,DEXTROMETHORPHAN HBR,DIPHENHYDRAMINE HCL, | TARGET CORPORATION | ce536313-7265-405c-88b7-f45e62781da5 | 2025-06-11 | Warnings | M012 |
| Capron Max | DEXTROMETHORPHAN HBR AND PYRILAMINE MALEATE | Capital Pharmaceutical, LLC | 3756812b-f128-8946-e063-6294a90a59ba | 2025-06-11 | Warnings | M012 |
| SAFETUSSIN Non Drowsy Cough plus chest congestion | DEXTROMETHORPHAN HYDROBROMIDE, AND GUAIFENESIN | KRAMER LABORATORIES | 60311ca3-8544-417e-aa29-e9f65c6692ba | 2025-06-11 | Warnings | M012 |
| Cold Max Nighttime | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | RETAIL BUSINESS SERVICES , LLC. | e65d2815-6932-123c-e053-2a95a90a2cf9 | 2025-06-10 | Warnings | M012 |
| Cold Head Congestion Daytime | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | American Sales Company | 0cc66c6c-db26-4bb2-a97d-c4106210d70c | 2025-06-10 | Warnings | M012 |
| Nighttime Cough DM | DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE | L.N.K. International, Inc. | 75a9c736-bc7e-4b7f-84ea-9474a37508ec | 2025-06-10 | Warnings | M012 |
| DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN | DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN | KJD Pharma Private Limited | 8877bb8d-479f-4968-8033-5c269d449a46 | 2025-06-10 | Warnings | M012 |
| Benadryl | DIPHENHYDRAMINE HYDROCHLORIDE | Morning Star OTC | f4ff84b3-bb0c-4900-8ba4-6d1b90394782 | 2025-06-09 | Warnings | M012 |
| Equate Kids Daytime Dex Cough Gels | DEXTROMETHORPHAN | Walmart | 37269cd6-1528-9879-e063-6394a90a2b54 | 2025-06-09 | Warnings | M012 |
| Nuvicare DayTime Cold and Flu Softgel | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | NUVICARE LLC | bdc35570-c8df-4797-a13e-7f2479ec42b7 | 2025-06-09 | Warnings | M012 |
| Nuvicare DayTime and NightTime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE | NUVICARE LLC | f5764925-c586-40e4-8252-24d92389af01 | 2025-06-09 | Warnings | M012 |
| Nuvicare NightTime Cold and Flu Softgel | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | NUVICARE LLC | 2a29f0ed-d86b-4787-84e0-f7a8c5e7581f | 2025-06-09 | Warnings | M012 |
| Nuvicare DayTime and NightTime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE | NUVICARE LLC | 7fa8e4ad-95cb-4905-90db-d53b3bc87c41 | 2025-06-09 | Warnings | M012 |
| Vaporizing Steam Liquid | MEDICATED COUGH SUPPRESSANT | NeilMed Pharmaceuticals Inc. | 36cf6218-adb8-9d8b-e063-6394a90a49a0 | 2025-06-05 | Warnings | M012 |
| Geri-Tussin DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | Geri-Care Pharmaceuticals, Corp | 7e2fb43c-a7f1-4c1d-a700-7c6510999c03 | 2025-06-05 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 310604 | guaiFENesin 100 MG in 5 mL Oral Solution | PSN | 312ce620-4841-7488-e054-00144ff88e88 | 9 |
| 310604 | guaifenesin 20 MG/ML Oral Solution | SCD | 312ce620-4841-7488-e054-00144ff88e88 | 9 |
| 310604 | guaifenesin 100 MG per 5 ML Oral Solution | SY | 312ce620-4841-7488-e054-00144ff88e88 | 9 |
| 310604 | guaifenesin 100 MG per 5 ML Oral Syrup | SY | 312ce620-4841-7488-e054-00144ff88e88 | 9 |
| 310604 | guaifenesin 200 MG per 10 ML Oral Solution | SY | 312ce620-4841-7488-e054-00144ff88e88 | 9 |
| 310604 | guaifenesin 300 MG per 15 ML Oral Solution | SY | 312ce620-4841-7488-e054-00144ff88e88 | 9 |
| 310604 | guaifenesin 400 MG per 20 ML Oral Solution | SY | 312ce620-4841-7488-e054-00144ff88e88 | 9 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 58657-509-16 | 58657050916 | 473 mL in 1 BOTTLE (58657-509-16) | 473 ml | 2016-02-09 | 0000-00-00 | No | No | Current |