Daytime Nighttime Sinus Relief Maximum Strength is a Kit in the Human Otc Drug category. It is labeled and distributed by Walgreens. The primary component is .
Product ID | 0363-0744_ddcb9a5c-e269-2c99-e053-2a95a90a3a35 |
NDC | 0363-0744 |
Product Type | Human Otc Drug |
Proprietary Name | Daytime Nighttime Sinus Relief Maximum Strength |
Generic Name | Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl/acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate,phenylephrine Hcl |
Dosage Form | Kit |
Marketing Start Date | 2022-06-01 |
Marketing Category | OTC MONOGRAPH FINAL / |
Application Number | part341 |
Labeler Name | Walgreens |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2022-06-01 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
69842-822 | Daytime Nighttime Sinus Relief Maximum Strength | Daytime Nighttime Sinus Relief Maximum Strength |
59779-554 | Daytime Nighttime Sinus Relief Maximum Strength | Daytime Nighttime Sinus Relief Maximum Strength |
0363-0622 | Daytime Nighttime Sinus Relief Maximum Strength | Daytime Nighttime Sinus Relief Maximum Strength |
0363-0723 | Daytime Nighttime Sinus Relief Maximum Strength | Daytime Nighttime Sinus Relief Maximum Strength |
69842-908 | Daytime Nighttime Sinus Relief Maximum Strength | Daytime Nighttime Sinus Relief Maximum Strength |
0363-0744 | Daytime Nighttime Sinus Relief | Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl/Acetaminophen, Dextromethorphan HBr, Doxylamine succinate,Phenylephrine HCl |