Product NDC: | 67234-020 |
Proprietary Name: | NATUREPLEX |
Non Proprietary Name: | (saline) |
Active Ingredient(s): | 7; 19 g/133mL; g/133mL & nbsp; (saline) |
Administration Route(s): | RECTAL |
Dosage Form(s): | ENEMA |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67234-020 |
Labeler Name: | Natureplex, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100601 |
Package NDC: | 67234-020-01 |
Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (67234-020-01) > 133 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Code | 67234-020-01 |
Proprietary Name | NATUREPLEX |
Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (67234-020-01) > 133 mL in 1 BOTTLE, WITH APPLICATOR |
Product NDC | 67234-020 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | (saline) |
Dosage Form Name | ENEMA |
Route Name | RECTAL |
Start Marketing Date | 20100601 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Natureplex, LLC |
Substance Name | SODIUM PHOSPHATE, DIBASIC; SODIUM PHOSPHATE, MONOBASIC |
Strength Number | 7; 19 |
Strength Unit | g/133mL; g/133mL |
Pharmaceutical Classes |