Product NDC: | 52686-255 |
Proprietary Name: | SHISEIDO WHITE LUCENT BRIGHTENING SPOT-CONTROL FOUNDATION (REFILL) |
Non Proprietary Name: | OCTINOXATE and TITANIUM DIOXIDE |
Active Ingredient(s): | .39; .66 g/10g; g/10g & nbsp; OCTINOXATE and TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52686-255 |
Labeler Name: | SHISEIDO AMERICA INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110301 |
Package NDC: | 52686-255-30 |
Package Description: | 1 TRAY in 1 CARTON (52686-255-30) > 10 g in 1 TRAY |
NDC Code | 52686-255-30 |
Proprietary Name | SHISEIDO WHITE LUCENT BRIGHTENING SPOT-CONTROL FOUNDATION (REFILL) |
Package Description | 1 TRAY in 1 CARTON (52686-255-30) > 10 g in 1 TRAY |
Product NDC | 52686-255 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE and TITANIUM DIOXIDE |
Dosage Form Name | PASTE |
Route Name | TOPICAL |
Start Marketing Date | 20110301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | SHISEIDO AMERICA INC. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | .39; .66 |
Strength Unit | g/10g; g/10g |
Pharmaceutical Classes |