Product NDC: | 13537-240 |
Proprietary Name: | LBEL |
Non Proprietary Name: | OCTINOXATE and OXYBENZONE |
Active Ingredient(s): | .075; .02 g/g; g/g & nbsp; OCTINOXATE and OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13537-240 |
Labeler Name: | Ventura Corporation (San Juan, P.R.) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100816 |
Package NDC: | 13537-240-02 |
Package Description: | 1 CASE in 1 BOX (13537-240-02) > 8 g in 1 CASE (13537-240-01) |
NDC Code | 13537-240-02 |
Proprietary Name | LBEL |
Package Description | 1 CASE in 1 BOX (13537-240-02) > 8 g in 1 CASE (13537-240-01) |
Product NDC | 13537-240 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE and OXYBENZONE |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20100816 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ventura Corporation (San Juan, P.R.) |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | .075; .02 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes |