Product NDC: | 30142-107 |
Proprietary Name: | Mucus Relief |
Non Proprietary Name: | Guaifenesin |
Active Ingredient(s): | 400 mg/1 & nbsp; Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 30142-107 |
Labeler Name: | The Kroger Co |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100706 |
Package NDC: | 30142-107-30 |
Package Description: | 1 BOTTLE in 1 BOX (30142-107-30) > 30 TABLET in 1 BOTTLE |
NDC Code | 30142-107-30 |
Proprietary Name | Mucus Relief |
Package Description | 1 BOTTLE in 1 BOX (30142-107-30) > 30 TABLET in 1 BOTTLE |
Product NDC | 30142-107 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100706 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | The Kroger Co |
Substance Name | GUAIFENESIN |
Strength Number | 400 |
Strength Unit | mg/1 |
Pharmaceutical Classes |