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DayTime Sinus Relief
DayTime Sinus Relief - 59995-006-00 - (ACETAMINOPHEN, PHENYLEPHRINE HCL)
Drug Information of DayTime Sinus Relief
| Product NDC: | 59995-006 |
| Proprietary Name: | DayTime Sinus Relief |
| Non Proprietary Name: | ACETAMINOPHEN, PHENYLEPHRINE HCL |
| Active Ingredient(s): | 325; 5 mg/1; mg/1 & nbsp; ACETAMINOPHEN, PHENYLEPHRINE HCL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DayTime Sinus Relief
| Product NDC: | 59995-006 |
| Labeler Name: | Robinson Pharma, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130612 |
Package Information of DayTime Sinus Relief
| Package NDC: | 59995-006-00 |
| Package Description: | 2 BLISTER PACK in 1 BOX (59995-006-00) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of DayTime Sinus Relief
| NDC Code | 59995-006-00 |
| Proprietary Name | DayTime Sinus Relief |
| Package Description | 2 BLISTER PACK in 1 BOX (59995-006-00) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 59995-006 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, PHENYLEPHRINE HCL |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20130612 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Robinson Pharma, Inc. |
| Substance Name | ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
