Product NDC: | 56062-234 |
Proprietary Name: | severe cold |
Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
Active Ingredient(s): | 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 56062-234 |
Labeler Name: | Publix Super Markets Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20071025 |
Package NDC: | 56062-234-62 |
Package Description: | 2 BLISTER PACK in 1 CARTON (56062-234-62) > 12 TABLET, COATED in 1 BLISTER PACK |
NDC Code | 56062-234-62 |
Proprietary Name | severe cold |
Package Description | 2 BLISTER PACK in 1 CARTON (56062-234-62) > 12 TABLET, COATED in 1 BLISTER PACK |
Product NDC | 56062-234 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20071025 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Publix Super Markets Inc |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 10; 200; 5 |
Strength Unit | mg/1; mg/1; mg/1; mg/1 |
Pharmaceutical Classes |