GUAIFENESIN DM is a Oral Syrup in the Human Otc Drug category. It is labeled and distributed by Cardinal Health. The primary component is Guaifenesin; Dextromethorphan.
| Product ID | 55154-5783_60c66bd6-a911-48d6-a26b-e7f928adbd66 |
| NDC | 55154-5783 |
| Product Type | Human Otc Drug |
| Proprietary Name | GUAIFENESIN DM |
| Generic Name | Guaifenesin And Dextromethorphan |
| Dosage Form | Syrup |
| Route of Administration | ORAL |
| Marketing Start Date | 1992-07-01 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Cardinal Health |
| Substance Name | GUAIFENESIN; DEXTROMETHORPHAN |
| Active Ingredient Strength | 100 mg/5mL; mg/5mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 1992-07-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1992-07-01 |
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 100 mg/5mL |
| SPL SET ID: | c5fd53c9-81d6-4ce6-88a0-c2c24e17a7ed |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0121-0638 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 0121-0809 | Guaifenesin DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 0121-1276 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 0121-4809 | Guaifenesin DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 43063-801 | Guaifenesin DM | Guaifenesin and Dextromethorphan Hydrobromide |
| 50090-2303 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 50090-3492 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 55154-5783 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 55154-5785 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 66007-204 | Expectorant plus Cough Relief | Guaifenesin and Dextromethorphan |
| 69822-021 | MMM - Cough Formula Guaifenesin DM | Guaifenesin DM |