AVAPTA - 76332-002-02 - (ALLANTOIN, HEXYLRESORCINOL, MENTHOL, WHITE CAMPHOR)

Alphabetical Index


Drug Information of AVAPTA

Product NDC: 76332-002
Proprietary Name: AVAPTA
Non Proprietary Name: ALLANTOIN, HEXYLRESORCINOL, MENTHOL, WHITE CAMPHOR
Active Ingredient(s): 5; 9; 1; 4    mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   ALLANTOIN, HEXYLRESORCINOL, MENTHOL, WHITE CAMPHOR
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of AVAPTA

Product NDC: 76332-002
Labeler Name: Neel Products LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120816

Package Information of AVAPTA

Package NDC: 76332-002-02
Package Description: 89 mL in 1 BOTTLE, SPRAY (76332-002-02)

NDC Information of AVAPTA

NDC Code 76332-002-02
Proprietary Name AVAPTA
Package Description 89 mL in 1 BOTTLE, SPRAY (76332-002-02)
Product NDC 76332-002
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALLANTOIN, HEXYLRESORCINOL, MENTHOL, WHITE CAMPHOR
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20120816
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Neel Products LLC
Substance Name ALLANTOIN; CAMPHOR (NATURAL); HEXYLRESORCINOL; MENTHOL
Strength Number 5; 9; 1; 4
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of AVAPTA


General Information