Product NDC: | 13537-011 |
Proprietary Name: | LBel |
Non Proprietary Name: | Octinoxate and Oxybenzone |
Active Ingredient(s): | .24; .06 g/4g; g/4g & nbsp; Octinoxate and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIPSTICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13537-011 |
Labeler Name: | VENTURA INTERNATIONAL LTD., |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100815 |
Package NDC: | 13537-011-62 |
Package Description: | 1 TUBE in 1 BOX (13537-011-62) > 4 g in 1 TUBE (13537-011-61) |
NDC Code | 13537-011-62 |
Proprietary Name | LBel |
Package Description | 1 TUBE in 1 BOX (13537-011-62) > 4 g in 1 TUBE (13537-011-61) |
Product NDC | 13537-011 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate and Oxybenzone |
Dosage Form Name | LIPSTICK |
Route Name | TOPICAL |
Start Marketing Date | 20100815 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | VENTURA INTERNATIONAL LTD., |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | .24; .06 |
Strength Unit | g/4g; g/4g |
Pharmaceutical Classes |