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Organix Complete
Organix Complete - 61941-0122-2 - (Menthol and Pectin)
Drug Information of Organix Complete
| Product NDC: | 61941-0122 |
| Proprietary Name: | Organix Complete |
| Non Proprietary Name: | Menthol and Pectin |
| Active Ingredient(s): | 2.5; 1.7 mg/1; mg/1 & nbsp; Menthol and Pectin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Organix Complete
| Product NDC: | 61941-0122 |
| Labeler Name: | ProPhase Labs, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101101 |
Package Information of Organix Complete
| Package NDC: | 61941-0122-2 |
| Package Description: | 48 PACKAGE in 1 CASE (61941-0122-2) > 21 LOZENGE in 1 PACKAGE (61941-0122-1) |
NDC Information of Organix Complete
| NDC Code | 61941-0122-2 |
| Proprietary Name | Organix Complete |
| Package Description | 48 PACKAGE in 1 CASE (61941-0122-2) > 21 LOZENGE in 1 PACKAGE (61941-0122-1) |
| Product NDC | 61941-0122 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol and Pectin |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20101101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | ProPhase Labs, Inc. |
| Substance Name | MENTHOL; PECTIN |
| Strength Number | 2.5; 1.7 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
