Product NDC: | 11822-0560 |
Proprietary Name: | Multi-Symptom Daytime Cold |
Non Proprietary Name: | Acetaminophen Phenylephrine HCl and Dextromethorphan HBr |
Active Ingredient(s): | 325; 10; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen Phenylephrine HCl and Dextromethorphan HBr |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-0560 |
Labeler Name: | Rite Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20080329 |
Package NDC: | 11822-0560-2 |
Package Description: | 1 BLISTER PACK in 1 CARTON (11822-0560-2) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Code | 11822-0560-2 |
Proprietary Name | Multi-Symptom Daytime Cold |
Package Description | 1 BLISTER PACK in 1 CARTON (11822-0560-2) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
Product NDC | 11822-0560 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen Phenylephrine HCl and Dextromethorphan HBr |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20080329 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Rite Aid Corporation |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 10; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |