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 |