| 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) |
| 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 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 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 |