Product NDC: | 22577-070 |
Proprietary Name: | AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE |
Non Proprietary Name: | AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE |
Active Ingredient(s): | .048; .192; .041 g/3.2g; g/3.2g; g/3.2g & nbsp; AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIPSTICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 22577-070 |
Labeler Name: | GRAFTON PRODUCTS CORP. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100223 |
Package NDC: | 22577-070-01 |
Package Description: | 3.2 g in 1 CONTAINER (22577-070-01) |
NDC Code | 22577-070-01 |
Proprietary Name | AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE |
Package Description | 3.2 g in 1 CONTAINER (22577-070-01) |
Product NDC | 22577-070 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE |
Dosage Form Name | LIPSTICK |
Route Name | TOPICAL |
Start Marketing Date | 20100223 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | GRAFTON PRODUCTS CORP. |
Substance Name | AVOBENZONE; OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | .048; .192; .041 |
Strength Unit | g/3.2g; g/3.2g; g/3.2g |
Pharmaceutical Classes |