NATUREPLEX - 67234-020-02 - ((saline))

Alphabetical Index


Drug Information of NATUREPLEX

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)

Labeler Information of NATUREPLEX

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 Information of NATUREPLEX

Package NDC: 67234-020-02
Package Description: 2 BOTTLE, WITH APPLICATOR in 1 CARTON (67234-020-02) > 133 mL in 1 BOTTLE, WITH APPLICATOR

NDC Information of NATUREPLEX

NDC Code 67234-020-02
Proprietary Name NATUREPLEX
Package Description 2 BOTTLE, WITH APPLICATOR in 1 CARTON (67234-020-02) > 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

Complete Information of NATUREPLEX


General Information