| 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 |