Product NDC: | 14783-011 |
Proprietary Name: | LBEL |
Non Proprietary Name: | OCTINOXATE, OXYBENZONE, and TITANIUM DIOXIDE |
Active Ingredient(s): | .07; .03; .008 g/g; g/g; g/g & nbsp; OCTINOXATE, OXYBENZONE, and TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIPSTICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 14783-011 |
Labeler Name: | Ventura International, Limited |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101215 |
Package NDC: | 14783-011-05 |
Package Description: | 1 TUBE in 1 CARTON (14783-011-05) > 4 g in 1 TUBE (14783-011-04) |
NDC Code | 14783-011-05 |
Proprietary Name | LBEL |
Package Description | 1 TUBE in 1 CARTON (14783-011-05) > 4 g in 1 TUBE (14783-011-04) |
Product NDC | 14783-011 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OXYBENZONE, and TITANIUM DIOXIDE |
Dosage Form Name | LIPSTICK |
Route Name | TOPICAL |
Start Marketing Date | 20101215 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ventura International, Limited |
Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
Strength Number | .07; .03; .008 |
Strength Unit | g/g; g/g; g/g |
Pharmaceutical Classes |