Pleo Ut - 60681-5301-2 - (bacillus subtilis)

Alphabetical Index


Drug Information of Pleo Ut

Product NDC: 60681-5301
Proprietary Name: Pleo Ut
Non Proprietary Name: bacillus subtilis
Active Ingredient(s): 6    [hp_X]/5mL & nbsp;   bacillus subtilis
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Pleo Ut

Product NDC: 60681-5301
Labeler Name: Sanum Kehlbeck GmbH & Co. KG
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19960319

Package Information of Pleo Ut

Package NDC: 60681-5301-2
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (60681-5301-2) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Pleo Ut

NDC Code 60681-5301-2
Proprietary Name Pleo Ut
Package Description 1 BOTTLE, DROPPER in 1 CARTON (60681-5301-2) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 60681-5301
Product Type Name HUMAN OTC DRUG
Non Proprietary Name bacillus subtilis
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 19960319
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Sanum Kehlbeck GmbH & Co. KG
Substance Name BACILLUS SUBTILIS
Strength Number 6
Strength Unit [hp_X]/5mL
Pharmaceutical Classes

Complete Information of Pleo Ut


General Information