Guaifed
- Product NDC
- 73564-801
- 11-digit product format
- 735640801
- Labeler code
- 73564
- Product ID
- 73564-801_58b32f6f-2554-884f-e063-6294a90a6bdd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Aldama Pharmaceuticals, Inc
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-06-01
- Substance
- GUAIFENESIN
- Active strength
- 200 mg/10mL
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- 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 | 73564-801 | 73564-801-08 | D | Discontinued by firm | 2026-10-21 | |
| excluded package | package | 73564-801 | 73564-801-16 | D | Discontinued by firm | 2026-10-21 |
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
- Guaifed
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 200 mg/10mL |
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 |
|---|---|
| 38f37272-2084-a33b-e063-6294a90ac150 | 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 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73564-801-04 | Guaifed | 118 mL in 1 BOTTLE | LIQUID | 118 | 5 | |
| 73564-801-08 | Guaifed | 237 mL in 1 BOTTLE | LIQUID | 237 | 5 | |
| 73564-801-16 | Guaifed | 473 mL in 1 BOTTLE | LIQUID | 473 | 5 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 73564-801-04 | ML - Milliliter | 73564-801 | c803fa57-88f5-436a-9f87-2509daa2fe85 | 1 | 2025-09-12 |
| 73564-801-08 | ML - Milliliter | 73564-801 | 8cc50634-6876-44cc-9558-f4a683da00af | 1 | 2025-09-12 |
| 73564-801-16 | ML - Milliliter | 73564-801 | ca0e6dd9-047e-4c1d-9c4d-7f75b8983cfb | 1 | 2025-09-12 |
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 |
|---|---|---|---|---|---|---|
| Daytime Cold and Flu Relief, 24-7 Life BY 7-Eleven | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL SOLUTION | Lil' Drug Store Products, Inc. | 2771d699-3f70-4318-e063-6394a90a89cc | 2025-12-09 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | Shield Pharmaceuticals Corp | 3d243264-5cd8-47da-9f5e-cfcfc8d1fa4b | 2025-12-09 | Warnings | M012 |
| Circle K Nighttime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE | Lil' Drug Store Products, Inc | 9a32bc6d-0499-48fa-a6ad-702c8a28bf5f | 2025-12-09 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | Shield Pharmaceuticals Corp | 5015a380-a229-4eff-8e31-528065c6ed64 | 2025-12-09 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | Harris Teeter | caf59320-5b48-4533-bda9-7b03a2fde0b5 | 2025-12-09 | Warnings | M012 |
| Sinus Severe | ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | STRATEGIC SOURCING SERVICES LLC | 30d41dc3-e2ef-4cad-b63c-d634bc749aa1 | 2025-12-09 | Warnings | M012 |
| Walgreens Childrens Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Walgreen Company | 327a7226-84b9-26d7-e063-6394a90a99b9 | 2025-12-09 | Warnings | M012 |
| Mucus Relief DM | DEXTROMETHORPHAN HBR AND GUAIFENESIN | Meijer Distribution Inc | 8ed5b802-a26e-45b4-a696-bc64dbac4733 | 2025-12-09 | Warnings | M012 |
| dg health cold plus flu relief | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Dolgencorp, LLC | ff4a2f0a-d638-4ed2-8e05-2a52afbc4909 | 2025-12-09 | Warnings | M012 |
| Daytime Cold and Flu | ACETAMINOPHEN DEXTROMETHORPHAN HBR PHENYLEPHRINE HCL | QUALITY CHOICE (Chain Drug Marketing Association) | 24894484-b834-4b2f-b365-c95b5e30d8bf | 2025-12-09 | Warnings | M012 |
| Nighttime Cold and Flu Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | Family Dollar (FAMILY WELLNESS) | 2c431220-c61b-4ad5-9ad2-58ccaee2d1c3 | 2025-12-09 | Warnings | M012 |
| Sinus PE Congestion Daytime Nighttime | DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL | Meijer Distribution, Inc. | 9da77306-5098-4c79-845c-97ead849c84a | 2025-12-08 | Warnings | M012 |
| Nighttime Cold and Flu Relief | ACETAMINOPHEN DEXTROMETHORPHAN HBR DOXYLAMINE SUCCINATE | QUALITY CHOICE (Chain Drug Marketing Association) | fdd0dadc-5313-4f6e-aef5-ca853efe5c4d | 2025-12-08 | Warnings | M012 |
| Mucolyte | GUAIFENESIN | Rising Pharma Holdings, Inc. | e4091aaf-44e3-4701-9986-aff248a2f1b8 | 2025-12-08 | Warnings | M012 |
| Mucolyte DM | GUAIFENESIN, DEXTROMETHORPHAN HBR | Rising Pharma Holdings, Inc. | c913d27d-bc00-4ace-9a5f-c55522e1cd1d | 2025-12-08 | Warnings | M012 |
| honey lemon cough drops | MENTHOL | American Sales | 47f504d5-3ec5-5227-e054-00144ff88e88 | 2025-12-07 | Warnings | M012 |
| Sugar Free Menthol Cough Drops | MENTHOL | American Sales | 4893ac0a-7769-5657-e054-00144ff8d46c | 2025-12-07 | Warnings | M012 |
| Cherry cough drop | MENTHOL | American Sales | 45e891ea-2f2a-31b7-e054-00144ff88e88 | 2025-12-07 | Warnings | M012 |
| Cherry Sore Throat Lozenge | BENZOCAINE | American Sales | 49248a40-1ca3-6dd1-e054-00144ff88e88 | 2025-12-07 | Warnings | M012 |
| Sugar Free Honey Lemon Cough Drops | MENTHOL | American Sales | 4896cbd1-57dd-1fc6-e054-00144ff8d46c | 2025-12-07 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 310604 | guaiFENesin 100 MG in 5 mL Oral Solution | PSN | 38f37272-2084-a33b-e063-6294a90ac150 | 6 |
| 310604 | guaifenesin 20 MG/ML Oral Solution | SCD | 38f37272-2084-a33b-e063-6294a90ac150 | 6 |
| 310604 | guaifenesin 100 MG per 5 ML Oral Solution | SY | 38f37272-2084-a33b-e063-6294a90ac150 | 6 |
| 310604 | guaifenesin 100 MG per 5 ML Oral Syrup | SY | 38f37272-2084-a33b-e063-6294a90ac150 | 6 |
| 310604 | guaifenesin 200 MG per 10 ML Oral Solution | SY | 38f37272-2084-a33b-e063-6294a90ac150 | 6 |
| 310604 | guaifenesin 300 MG per 15 ML Oral Solution | SY | 38f37272-2084-a33b-e063-6294a90ac150 | 6 |
| 310604 | guaifenesin 400 MG per 20 ML Oral Solution | SY | 38f37272-2084-a33b-e063-6294a90ac150 | 6 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 73564-801-04 | 73564080104 | 118 mL in 1 BOTTLE (73564-801-04) | 118 ml | 2026-06-01 | No | No | Current |
| 73564-801-08 | 73564080108 | 237 mL in 1 BOTTLE | 237 ml | Historical | |||
| 73564-801-16 | 73564080116 | 473 mL in 1 BOTTLE | 473 ml | Historical |