Product NDC: | 53345-013 |
Proprietary Name: | NightTime Sinus Relief |
Non Proprietary Name: | Acetaminophen, Doxylamine succinate, Phenylephrine hydrochloride |
Active Ingredient(s): | 325; 6.25; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Doxylamine succinate, Phenylephrine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53345-013 |
Labeler Name: | Humanwell PuraCap Pharmaceutical (Wuhan), Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130615 |
Package NDC: | 53345-013-01 |
Package Description: | 1 BAG in 1 BOX (53345-013-01) > 4000 CAPSULE, LIQUID FILLED in 1 BAG |
NDC Code | 53345-013-01 |
Proprietary Name | NightTime Sinus Relief |
Package Description | 1 BAG in 1 BOX (53345-013-01) > 4000 CAPSULE, LIQUID FILLED in 1 BAG |
Product NDC | 53345-013 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Doxylamine succinate, Phenylephrine hydrochloride |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20130615 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Humanwell PuraCap Pharmaceutical (Wuhan), Ltd. |
Substance Name | ACETAMINOPHEN; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 6.25; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |