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Kids-EEZE
Kids-EEZE - 61941-1002-1 - (Guaifenesin)
Drug Information of Kids-EEZE
| Product NDC: | 61941-1002 |
| Proprietary Name: | Kids-EEZE |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 100 mg/1 & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kids-EEZE
| Product NDC: | 61941-1002 |
| Labeler Name: | ProPhase Labs, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080901 |
Package Information of Kids-EEZE
| Package NDC: | 61941-1002-1 |
| Package Description: | 72 PACKAGE in 1 CASE (61941-1002-1) > 12 TABLET, ORALLY DISINTEGRATING in 1 PACKAGE (61941-1002-6) |
NDC Information of Kids-EEZE
| NDC Code | 61941-1002-1 |
| Proprietary Name | Kids-EEZE |
| Package Description | 72 PACKAGE in 1 CASE (61941-1002-1) > 12 TABLET, ORALLY DISINTEGRATING in 1 PACKAGE (61941-1002-6) |
| Product NDC | 61941-1002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20080901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | ProPhase Labs, Inc. |
| Substance Name | GUAIFENESIN |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
