Bodycology - 51706-305-02 - (Alcohol)

Alphabetical Index


Drug Information of Bodycology

Product NDC: 51706-305
Proprietary Name: Bodycology
Non Proprietary Name: Alcohol
Active Ingredient(s): 70    mL/100mL & nbsp;   Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Bodycology

Product NDC: 51706-305
Labeler Name: Landy International
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100630

Package Information of Bodycology

Package NDC: 51706-305-02
Package Description: 1 BOTTLE in 1 PACKAGE (51706-305-02) > 55 mL in 1 BOTTLE (51706-305-01)

NDC Information of Bodycology

NDC Code 51706-305-02
Proprietary Name Bodycology
Package Description 1 BOTTLE in 1 PACKAGE (51706-305-02) > 55 mL in 1 BOTTLE (51706-305-01)
Product NDC 51706-305
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Alcohol
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20100630
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Landy International
Substance Name ALCOHOL
Strength Number 70
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Bodycology


General Information