O BlancTis - 47649-6001-2 - (alcohol)

Alphabetical Index


Drug Information of O BlancTis

Product NDC: 47649-6001
Proprietary Name: O BlancTis
Non Proprietary Name: alcohol
Active Ingredient(s): 50    g/100g & nbsp;   alcohol
Administration Route(s): DENTAL
Dosage Form(s): GEL, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of O BlancTis

Product NDC: 47649-6001
Labeler Name: Nibec Co., Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120207

Package Information of O BlancTis

Package NDC: 47649-6001-2
Package Description: 3 TUBE in 1 BOX (47649-6001-2) > 5 g in 1 TUBE (47649-6001-1)

NDC Information of O BlancTis

NDC Code 47649-6001-2
Proprietary Name O BlancTis
Package Description 3 TUBE in 1 BOX (47649-6001-2) > 5 g in 1 TUBE (47649-6001-1)
Product NDC 47649-6001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name alcohol
Dosage Form Name GEL, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20120207
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Nibec Co., Ltd
Substance Name ALCOHOL
Strength Number 50
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of O BlancTis


General Information