Product NDC: | 63824-473 |
Proprietary Name: | Childrens Mucinex |
Non Proprietary Name: | Guaifenesin |
Active Ingredient(s): | 100 mg/5mL & nbsp; Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63824-473 |
Labeler Name: | Reckitt Benckiser, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100622 |
Package NDC: | 63824-473-64 |
Package Description: | 1 BOTTLE in 1 CARTON (63824-473-64) > 118 mL in 1 BOTTLE |
NDC Code | 63824-473-64 |
Proprietary Name | Childrens Mucinex |
Package Description | 1 BOTTLE in 1 CARTON (63824-473-64) > 118 mL in 1 BOTTLE |
Product NDC | 63824-473 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20100622 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Reckitt Benckiser, Inc. |
Substance Name | GUAIFENESIN |
Strength Number | 100 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |