Product NDC: | 63824-214 |
Proprietary Name: | Childrens Delsym |
Non Proprietary Name: | Dextromethorphan Hydrobromide and Guaifenesin |
Active Ingredient(s): | 5; 100 mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide and Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63824-214 |
Labeler Name: | Reckitt Benckiser LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130331 |
Package NDC: | 63824-214-66 |
Package Description: | 180 mL in 1 BOTTLE (63824-214-66) |
NDC Code | 63824-214-66 |
Proprietary Name | Childrens Delsym |
Package Description | 180 mL in 1 BOTTLE (63824-214-66) |
Product NDC | 63824-214 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan Hydrobromide and Guaifenesin |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20130331 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Reckitt Benckiser LLC |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 5; 100 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |