Home > National Drug Code (NDC) > U-max Multi BB

U-max Multi BB - 50795-2001-1 - (ALLANTOIN)

Alphabetical Index


Drug Information of U-max Multi BB

Product NDC: 50795-2001
Proprietary Name: U-max Multi BB
Non Proprietary Name: ALLANTOIN
Active Ingredient(s): .1    mL/100mL & nbsp;   ALLANTOIN
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of U-max Multi BB

Product NDC: 50795-2001
Labeler Name: VS Shinbi Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120604

Package Information of U-max Multi BB

Package NDC: 50795-2001-1
Package Description: 30 mL in 1 BOTTLE, WITH APPLICATOR (50795-2001-1)

NDC Information of U-max Multi BB

NDC Code 50795-2001-1
Proprietary Name U-max Multi BB
Package Description 30 mL in 1 BOTTLE, WITH APPLICATOR (50795-2001-1)
Product NDC 50795-2001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALLANTOIN
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120604
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name VS Shinbi Co., Ltd.
Substance Name ALLANTOIN
Strength Number .1
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of U-max Multi BB


General Information