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BlancTis Forte II - 47649-5001-4 - (alcohol)

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Drug Information of BlancTis Forte II

Product NDC: 47649-5001
Proprietary Name: BlancTis Forte II
Non Proprietary Name: alcohol
Active Ingredient(s): 500    mg/g & nbsp;   alcohol
Administration Route(s): DENTAL
Dosage Form(s): GEL, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of BlancTis Forte II

Product NDC: 47649-5001
Labeler Name: Nibec Co., Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100724

Package Information of BlancTis Forte II

Package NDC: 47649-5001-4
Package Description: 2 CARTON in 1 CARTON (47649-5001-4) > 4 TUBE in 1 CARTON (47649-5001-3) > 3 g in 1 TUBE (47649-5001-2)

NDC Information of BlancTis Forte II

NDC Code 47649-5001-4
Proprietary Name BlancTis Forte II
Package Description 2 CARTON in 1 CARTON (47649-5001-4) > 4 TUBE in 1 CARTON (47649-5001-3) > 3 g in 1 TUBE (47649-5001-2)
Product NDC 47649-5001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name alcohol
Dosage Form Name GEL, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20100724
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Nibec Co., Ltd
Substance Name ALCOHOL
Strength Number 500
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of BlancTis Forte II


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