| Product NDC: | 36800-102 |
| Proprietary Name: | DayTime Nitetime 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: | 36800-102 |
| Labeler Name: | TOP CARE (Topco Associates LLC) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130115 |
| Package NDC: | 36800-102-48 |
| Package Description: | 1 KIT in 1 CARTON (36800-102-48) * 8 CAPSULE in 1 BLISTER PACK * 8 CAPSULE in 1 BLISTER PACK |
| NDC Code | 36800-102-48 |
| Proprietary Name | DayTime Nitetime Sinus Relief |
| Package Description | 1 KIT in 1 CARTON (36800-102-48) * 8 CAPSULE in 1 BLISTER PACK * 8 CAPSULE in 1 BLISTER PACK |
| Product NDC | 36800-102 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Doxylamine succinate, Phenylephrine HCl |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130115 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | TOP CARE (Topco Associates LLC) |
| Substance Name | |
| Strength Number | |
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