Sinus Max Relief Day and Night is a Kit in the Human Otc Drug category. It is labeled and distributed by Topco Associates Llc. The primary component is .
Product ID | 36800-765_87564316-4956-46a9-8e8f-6e784a79865b |
NDC | 36800-765 |
Product Type | Human Otc Drug |
Proprietary Name | Sinus Max Relief Day and Night |
Generic Name | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succinate, And Phenylephrine Hydrochloride |
Dosage Form | Kit |
Marketing Start Date | 2021-05-01 |
Marketing Category | OTC MONOGRAPH FINAL / |
Application Number | part341 |
Labeler Name | TOPCO ASSOCIATES LLC |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2021-05-01 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
36800-765 | Sinus Max Relief Day and Night | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succinate, and Phenylephrine Hydrochloride |
36800-746 | Cold and Flu Severe Daytime/Nighttime | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succinate, and Phenylephrine Hydrochloride |
72854-129 | Mucinex Fast-Max Day Cold and Flu and Night Cold and Flu | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succinate, and Phenylephrine Hydrochloride |
72854-204 | Mucinex Sinus-Max Day and Night | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succinate, and Phenylephrine Hydrochloride |