Product NDC: | 50804-101 |
Proprietary Name: | Nighttime sinus |
Non Proprietary Name: | Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride |
Active Ingredient(s): | 325; 6.25; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50804-101 |
Labeler Name: | Geiss, Destin & Dunn, Inc (Goodsense) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120701 |
Package NDC: | 50804-101-24 |
Package Description: | 2 BLISTER PACK in 1 CARTON (50804-101-24) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Code | 50804-101-24 |
Proprietary Name | Nighttime sinus |
Package Description | 2 BLISTER PACK in 1 CARTON (50804-101-24) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
Product NDC | 50804-101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20120701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Geiss, Destin & Dunn, Inc (Goodsense) |
Substance Name | ACETAMINOPHEN; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 6.25; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |