Product NDC: | 0904-5792 |
Proprietary Name: | Sinus Congestion PE |
Non Proprietary Name: | Guaifenesin and Phenylephrine HCl |
Active Ingredient(s): | 400; 10 mg/1; mg/1 & nbsp; Guaifenesin and Phenylephrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-5792 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20060415 |
Package NDC: | 0904-5792-01 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0904-5792-01) > 30 TABLET in 1 BOTTLE, PLASTIC |
NDC Code | 0904-5792-01 |
Proprietary Name | Sinus Congestion PE |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0904-5792-01) > 30 TABLET in 1 BOTTLE, PLASTIC |
Product NDC | 0904-5792 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin and Phenylephrine HCl |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20060415 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Major Pharmaceuticals |
Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 400; 10 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |