| Product NDC: | 61715-011 |
| Proprietary Name: | Sinus Congestion and Pain Severe |
| Non Proprietary Name: | ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 325; 200; 5 mg/1; mg/1; mg/1 & nbsp; ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61715-011 |
| Labeler Name: | Kinray Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130509 |
| Package NDC: | 61715-011-24 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (61715-011-24) > 12 TABLET, COATED in 1 BLISTER PACK |
| NDC Code | 61715-011-24 |
| Proprietary Name | Sinus Congestion and Pain Severe |
| Package Description | 2 BLISTER PACK in 1 CARTON (61715-011-24) > 12 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 61715-011 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130509 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kinray Inc. |
| Substance Name | ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 200; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |