LBEL - 14783-880-08 - (OCTINOXATE and OXYBENZONE)

Alphabetical Index


Drug Information of LBEL

Product NDC: 14783-880
Proprietary Name: LBEL
Non Proprietary Name: OCTINOXATE and OXYBENZONE
Active Ingredient(s): .07; .03    mL/mL; mL/mL & nbsp;   OCTINOXATE and OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LIPSTICK
Coding System: National Drug Codes(NDC)

Labeler Information of LBEL

Product NDC: 14783-880
Labeler Name: Ventura International, Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20101205

Package Information of LBEL

Package NDC: 14783-880-08
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (14783-880-08) > 7 mL in 1 TUBE, WITH APPLICATOR (14783-880-07)

NDC Information of LBEL

NDC Code 14783-880-08
Proprietary Name LBEL
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (14783-880-08) > 7 mL in 1 TUBE, WITH APPLICATOR (14783-880-07)
Product NDC 14783-880
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE and OXYBENZONE
Dosage Form Name LIPSTICK
Route Name TOPICAL
Start Marketing Date 20101205
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ventura International, Limited
Substance Name OCTINOXATE; OXYBENZONE
Strength Number .07; .03
Strength Unit mL/mL; mL/mL
Pharmaceutical Classes

Complete Information of LBEL


General Information