Product NDC: | 55910-455 |
Proprietary Name: | Allergy Multi-Symptom |
Non Proprietary Name: | Acetaminophen, Chlorpheniramine Maleate and Phenylephrine HCl |
Active Ingredient(s): | 325; 2; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Chlorpheniramine Maleate and Phenylephrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55910-455 |
Labeler Name: | DOLGENCORP, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20060530 |
Package NDC: | 55910-455-08 |
Package Description: | 1 BLISTER PACK in 1 CARTON (55910-455-08) > 24 TABLET in 1 BLISTER PACK |
NDC Code | 55910-455-08 |
Proprietary Name | Allergy Multi-Symptom |
Package Description | 1 BLISTER PACK in 1 CARTON (55910-455-08) > 24 TABLET in 1 BLISTER PACK |
Product NDC | 55910-455 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Chlorpheniramine Maleate and Phenylephrine HCl |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20060530 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | DOLGENCORP, LLC |
Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 2; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |