| Product NDC: | 0363-1019 |
| Proprietary Name: | Day Time Night Time Sinus Relief |
| Non Proprietary Name: | Acetaminophen, Doxylamine succinate, Phenylephrine HCl |
| Active Ingredient(s): | & nbsp; Acetaminophen, Doxylamine succinate, Phenylephrine HCl |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0363-1019 |
| Labeler Name: | Walgeens Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130301 |
| Package NDC: | 0363-1019-03 |
| Package Description: | 1 KIT in 1 CARTON (0363-1019-03) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| NDC Code | 0363-1019-03 |
| Proprietary Name | Day Time Night Time Sinus Relief |
| Package Description | 1 KIT in 1 CARTON (0363-1019-03) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 0363-1019 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Doxylamine succinate, Phenylephrine HCl |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Walgeens Company |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |