Bodycology - 51706-201-02 - (Ethyl Alcohol)

Alphabetical Index


Drug Information of Bodycology

Product NDC: 51706-201
Proprietary Name: Bodycology
Non Proprietary Name: Ethyl Alcohol
Active Ingredient(s): 65    mL/100mL & nbsp;   Ethyl Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Bodycology

Product NDC: 51706-201
Labeler Name: Landy International
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100625

Package Information of Bodycology

Package NDC: 51706-201-02
Package Description: 1 BOTTLE in 1 BOX (51706-201-02) > 30 mL in 1 BOTTLE (51706-201-01)

NDC Information of Bodycology

NDC Code 51706-201-02
Proprietary Name Bodycology
Package Description 1 BOTTLE in 1 BOX (51706-201-02) > 30 mL in 1 BOTTLE (51706-201-01)
Product NDC 51706-201
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ethyl Alcohol
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20100625
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Landy International
Substance Name ALCOHOL
Strength Number 65
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Bodycology


General Information