Home > National Drug Code (NDC) > BETULA ALBA JUICE WHITE GEL

BETULA ALBA JUICE WHITE GEL - 76214-026-01 - (DIMETHICONE)

Alphabetical Index


Drug Information of BETULA ALBA JUICE WHITE GEL

Product NDC: 76214-026
Proprietary Name: BETULA ALBA JUICE WHITE GEL
Non Proprietary Name: DIMETHICONE
Active Ingredient(s): 2.72    g/50g & nbsp;   DIMETHICONE
Administration Route(s): CUTANEOUS
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of BETULA ALBA JUICE WHITE GEL

Product NDC: 76214-026
Labeler Name: SKINFOOD CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110301

Package Information of BETULA ALBA JUICE WHITE GEL

Package NDC: 76214-026-01
Package Description: 50 g in 1 BOTTLE (76214-026-01)

NDC Information of BETULA ALBA JUICE WHITE GEL

NDC Code 76214-026-01
Proprietary Name BETULA ALBA JUICE WHITE GEL
Package Description 50 g in 1 BOTTLE (76214-026-01)
Product NDC 76214-026
Product Type Name HUMAN OTC DRUG
Non Proprietary Name DIMETHICONE
Dosage Form Name CREAM
Route Name CUTANEOUS
Start Marketing Date 20110301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name SKINFOOD CO., LTD.
Substance Name DIMETHICONE
Strength Number 2.72
Strength Unit g/50g
Pharmaceutical Classes

Complete Information of BETULA ALBA JUICE WHITE GEL


General Information