CounterAct Day is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Melaleuca, Inc.. The primary component is Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride.
Product ID | 54473-185_65e42ef2-d090-6174-e053-2991aa0a9830 |
NDC | 54473-185 |
Product Type | Human Otc Drug |
Proprietary Name | CounterAct Day |
Generic Name | Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2011-10-01 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part341 |
Labeler Name | Melaleuca, Inc. |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Active Ingredient Strength | 325 mg/1; mg/1; mg/1; mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2018-01-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-01-01 |
Marketing End Date | 2019-12-31 |
Ingredient | Strength |
---|---|
ACETAMINOPHEN | 325 mg/1 |
SPL SET ID: | 07ee5376-e907-4183-b49a-67f5e894836c |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |