Product NDC: | 0132-0202 |
Proprietary Name: | Pedia-Lax |
Non Proprietary Name: | sodium phosphate, dibasic and sodium phosphate, monobasic |
Active Ingredient(s): | 3.5; 9.5 g/66mL; g/66mL & nbsp; sodium phosphate, dibasic and sodium phosphate, monobasic |
Administration Route(s): | RECTAL |
Dosage Form(s): | ENEMA |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0132-0202 |
Labeler Name: | C.B. Fleet Company, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20020510 |
Package NDC: | 0132-0202-20 |
Package Description: | 66 mL in 1 BOTTLE, WITH APPLICATOR (0132-0202-20) |
NDC Code | 0132-0202-20 |
Proprietary Name | Pedia-Lax |
Package Description | 66 mL in 1 BOTTLE, WITH APPLICATOR (0132-0202-20) |
Product NDC | 0132-0202 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | sodium phosphate, dibasic and sodium phosphate, monobasic |
Dosage Form Name | ENEMA |
Route Name | RECTAL |
Start Marketing Date | 20020510 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | C.B. Fleet Company, Inc. |
Substance Name | SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC |
Strength Number | 3.5; 9.5 |
Strength Unit | g/66mL; g/66mL |
Pharmaceutical Classes |