Product NDC: | 41250-903 |
Proprietary Name: | Pain Relief Plus |
Non Proprietary Name: | Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan HBr, Phenylephrine HCl |
Active Ingredient(s): | 160; 1; 5; 2.5 mg/5mL; mg/5mL; mg/5mL; mg/5mL & nbsp; Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan HBr, Phenylephrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41250-903 |
Labeler Name: | Meijer Distribution Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20080801 |
Package NDC: | 41250-903-26 |
Package Description: | 1 BOTTLE in 1 CARTON (41250-903-26) > 118 mL in 1 BOTTLE |
NDC Code | 41250-903-26 |
Proprietary Name | Pain Relief Plus |
Package Description | 1 BOTTLE in 1 CARTON (41250-903-26) > 118 mL in 1 BOTTLE |
Product NDC | 41250-903 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan HBr, Phenylephrine HCl |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20080801 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Meijer Distribution Inc |
Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 160; 1; 5; 2.5 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL; mg/5mL |
Pharmaceutical Classes |