Home > National Drug Code (NDC) > LBEL HYDRATESS

LBEL HYDRATESS - 13537-525-02 - (Octinoxate and Oxybenzone)

Alphabetical Index


Drug Information of LBEL HYDRATESS

Product NDC: 13537-525
Proprietary Name: LBEL HYDRATESS
Non Proprietary Name: Octinoxate and Oxybenzone
Active Ingredient(s): .071; .016    g/g; g/g & nbsp;   Octinoxate and Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LIPSTICK
Coding System: National Drug Codes(NDC)

Labeler Information of LBEL HYDRATESS

Product NDC: 13537-525
Labeler Name: Ventura Corporation LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130527

Package Information of LBEL HYDRATESS

Package NDC: 13537-525-02
Package Description: 1 TUBE in 1 BOX (13537-525-02) > 4 g in 1 TUBE (13537-525-01)

NDC Information of LBEL HYDRATESS

NDC Code 13537-525-02
Proprietary Name LBEL HYDRATESS
Package Description 1 TUBE in 1 BOX (13537-525-02) > 4 g in 1 TUBE (13537-525-01)
Product NDC 13537-525
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate and Oxybenzone
Dosage Form Name LIPSTICK
Route Name TOPICAL
Start Marketing Date 20130527
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ventura Corporation LTD.
Substance Name OCTINOXATE; OXYBENZONE
Strength Number .071; .016
Strength Unit g/g; g/g
Pharmaceutical Classes

Complete Information of LBEL HYDRATESS


General Information