DOMETUSS-DMX is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Domel Laboratories. The primary component is Guaifenesin; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride.
| Product ID | 53809-203_23161838-5b4c-42c1-b8b6-653d26334fda |
| NDC | 53809-203 |
| Product Type | Human Otc Drug |
| Proprietary Name | DOMETUSS-DMX |
| Generic Name | Guaifenesin, Dextromethorphan Hbr, Phenylephrine Hcl |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-01-21 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Domel Laboratories |
| Substance Name | GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient Strength | 200 mg/5mL; mg/5mL; mg/5mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2016-01-21 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-01-21 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2016-01-21 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-01-21 |
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 200 mg/5mL |
| SPL SET ID: | 6949e1c6-df1c-451b-a1e2-9199415440f4 |
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| UNII | |
| RxNorm Concept Unique ID - RxCUI |