Product NDC: | 63824-254 |
Proprietary Name: | Childrens Mucinex |
Non Proprietary Name: | Guaifenesin |
Active Ingredient(s): | 100 mg/1 & nbsp; Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | GRANULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63824-254 |
Labeler Name: | Reckitt Benckiser |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090324 |
Package NDC: | 63824-254-12 |
Package Description: | 12 PACKET in 1 CARTON (63824-254-12) > 1 GRANULE in 1 PACKET |
NDC Code | 63824-254-12 |
Proprietary Name | Childrens Mucinex |
Package Description | 12 PACKET in 1 CARTON (63824-254-12) > 1 GRANULE in 1 PACKET |
Product NDC | 63824-254 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin |
Dosage Form Name | GRANULE |
Route Name | ORAL |
Start Marketing Date | 20090324 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Reckitt Benckiser |
Substance Name | GUAIFENESIN |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes |