Pleo Ut - 60681-5305-2 - (bacillus subtilis)

Alphabetical Index


Drug Information of Pleo Ut

Product NDC: 60681-5305
Proprietary Name: Pleo Ut
Non Proprietary Name: bacillus subtilis
Active Ingredient(s): 4    [hp_X]/mL & nbsp;   bacillus subtilis
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Pleo Ut

Product NDC: 60681-5305
Labeler Name: Sanum Kehlbeck GmbH & Co. KG
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19970319

Package Information of Pleo Ut

Package NDC: 60681-5305-2
Package Description: 50 VIAL, GLASS in 1 CARTON (60681-5305-2) > 1 mL in 1 VIAL, GLASS

NDC Information of Pleo Ut

NDC Code 60681-5305-2
Proprietary Name Pleo Ut
Package Description 50 VIAL, GLASS in 1 CARTON (60681-5305-2) > 1 mL in 1 VIAL, GLASS
Product NDC 60681-5305
Product Type Name HUMAN OTC DRUG
Non Proprietary Name bacillus subtilis
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19970319
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Sanum Kehlbeck GmbH & Co. KG
Substance Name BACILLUS SUBTILIS
Strength Number 4
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of Pleo Ut


General Information