Pedia-Lax - 0132-0202-20 - (sodium phosphate, dibasic and sodium phosphate, monobasic)

Alphabetical Index


Drug Information of Pedia-Lax

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)

Labeler Information of Pedia-Lax

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 Information of Pedia-Lax

Package NDC: 0132-0202-20
Package Description: 66 mL in 1 BOTTLE, WITH APPLICATOR (0132-0202-20)

NDC Information of Pedia-Lax

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

Complete Information of Pedia-Lax


General Information