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 |
|---|---|---|---|---|---|---|
| MULTI-SYMPTOM COLD | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Family Dollar Services Inc | b1fae7cc-4033-44bc-aa7c-ca3ceea51c7d | 2025-11-15 | Warnings | M012 |
| Cold and Flu Severe | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Rite Aid Corporation | 1affbef6-dd27-40c2-a5d3-b121aa62496a | 2025-11-15 | Warnings | M012 |
| Cold and Flu Day, Night | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Walgreen Company | b9adfb5d-6576-4ff8-a7d7-a89b867c5292 | 2025-11-14 | Warnings | M012 |
| PECGEN DMX | DEXTROMETHORPHAN HBR, GUAIFENESIN | KRAMER NOVIS | a627824c-5e3d-4672-a047-6c801b50b432 | 2025-11-14 | Warnings | M012 |
| Supress DM | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN | KRAMER NOVIS | 7da0611e-729c-4cf8-88f3-f8877b9f5cfa | 2025-11-14 | Warnings | M012 |
| G-ZYNCOF | DEXTROMETHORPHAN HBR AND GUAIFENESIN | Kramer Novis | c1aa7060-0f32-4ea1-8e2e-1aa131bd55fc | 2025-11-14 | Warnings | M012 |
| equate vapor ice cold and flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | Wal-Mart Stores Inc | b2c0692c-ed0b-4fcf-b88d-59a788b124c6 | 2025-11-14 | Warnings | M012 |
| Guaifenesin 400mg | GUAIFENESIN | Marlex Pharmaceuticals Inc | 13f4db4e-687e-9d7b-e063-6294a90ab088 | 2025-11-13 | Warnings | M012 |
| Guaifenesin 200mg | GUAIFENESIN | Marlex Pharmaceuticals Inc | 13b8f480-d1ac-d70c-e063-6394a90ab4f4 | 2025-11-13 | Warnings | M012 |
| Diphenhydramine HCL | DIPHENHYDRAMINE HCL | PD-Rx Pharmaceuticals, Inc. | c1873a4c-661f-4896-bcc0-f6d3a655de94 | 2025-11-13 | Warnings | M012 |
| Theraflu Severe Cold Relief Nighttime | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | Haleon US Holdings LLC | c24b9489-208c-472b-8ae5-c6e86c12e04d | 2025-11-13 | Warnings | M012 |
| Theraflu Severe Cold Relief Chest Congestion Daytime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN | Haleon US Holdings LLC | 8c821671-dc68-4e27-aa87-b4e45ade9817 | 2025-11-13 | Warnings | M012 |
| Robitussin Maximum Strength Severe Cough Plus Sore Throat | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE | Haleon US Holdings LLC | 6a6f5da8-6433-4284-8df7-2d5b099b74dc | 2025-11-13 | Warnings | M012 |
| equaline allergy | DIPHENHYDRAMINE HCL | United Natural Foods, Inc. dba UNFI | 8e4eb1eb-5b55-4531-94d2-998425ec80ed | 2025-11-13 | Warnings | M012 |
| Cold and Flu DayTime | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Safeway, Inc. | 7a78f24b-7c23-4318-99dc-90c05db185b1 | 2025-11-13 | Warnings | M012 |
| ZYNCOF | DEXTROMETHORPHAN HBR AND GUAIFENESIN | Kramer Novis | cffd6d5f-0cb2-4d38-bdb0-6a21120418cc | 2025-11-13 | Warnings | M012 |
| equate vapor ice cold and flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Wal-Mart Stores Inc | b6da1659-8c79-4cce-a817-907a7f061a2d | 2025-11-13 | Warnings | M012 |
| Tussi Pres | GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE | Kramer Novis | 0d4ee530-2a5c-41a0-88bf-ac92d538661b | 2025-11-12 | Warnings | M012 |
| 4 Way Fast Acting | PHENYLEPHRINE HYDROCHLORIDE | Haleon US Holdings LLC | a8fc41c7-4425-41b8-b1c6-eb22ac054734 | 2025-11-12 | Warnings | M012 |
| Quality Choice Vapor Steam | CAMPHOR (SYNTHETIC) | Chain Drug Marketing Association, Inc. | 1f1e6be5-d407-330c-e063-6294a90a4e80 | 2025-11-12 | 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 |