| Product NDC: | 46084-101 |
| Proprietary Name: | ACETAMINOPHEN SINUS CONGESTION AND PAIN |
| 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): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 46084-101 |
| Labeler Name: | A P J Laboratories Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130606 |
| Package NDC: | 46084-101-30 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (46084-101-30) |
| NDC Code | 46084-101-30 |
| Proprietary Name | ACETAMINOPHEN SINUS CONGESTION AND PAIN |
| Package Description | 30 TABLET in 1 BLISTER PACK (46084-101-30) |
| Product NDC | 46084-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130606 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | A P J Laboratories Limited |
| Substance Name | ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |