Product NDC: | 56062-964 |
Proprietary Name: | flu and severe cold and cough |
Non Proprietary Name: | Acetaminophen, Diphenhydramine hydrochloride, Phenylephrine hydrochloride |
Active Ingredient(s): | 650; 25; 10 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine hydrochloride, Phenylephrine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 56062-964 |
Labeler Name: | Publix Super Markets Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110929 |
Package NDC: | 56062-964-91 |
Package Description: | 6 POWDER, FOR SOLUTION in 1 CARTON (56062-964-91) |
NDC Code | 56062-964-91 |
Proprietary Name | flu and severe cold and cough |
Package Description | 6 POWDER, FOR SOLUTION in 1 CARTON (56062-964-91) |
Product NDC | 56062-964 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Diphenhydramine hydrochloride, Phenylephrine hydrochloride |
Dosage Form Name | POWDER, FOR SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20110929 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Publix Super Markets Inc |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 650; 25; 10 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |