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DayTime Sinus Relief
DayTime Sinus Relief - 53345-012-01 - (acetaminophen, phenylephrine hydrochloride)
Drug Information of DayTime Sinus Relief
| Product NDC: | 53345-012 |
| Proprietary Name: | DayTime Sinus Relief |
| Non Proprietary Name: | acetaminophen, phenylephrine hydrochloride |
| Active Ingredient(s): | 325; 5 mg/1; mg/1 & nbsp; acetaminophen, phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DayTime Sinus Relief
| Product NDC: | 53345-012 |
| 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 Information of DayTime Sinus Relief
| Package NDC: | 53345-012-01 |
| Package Description: | 1 BAG in 1 BOX (53345-012-01) > 4000 CAPSULE, LIQUID FILLED in 1 BAG |
NDC Information of DayTime Sinus Relief
| NDC Code | 53345-012-01 |
| Proprietary Name | DayTime Sinus Relief |
| Package Description | 1 BAG in 1 BOX (53345-012-01) > 4000 CAPSULE, LIQUID FILLED in 1 BAG |
| Product NDC | 53345-012 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen, 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; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
