Product NDC: | 52686-224 |
Proprietary Name: | SHISEIDO SUNCARE ULTIMATE |
Non Proprietary Name: | Octinoxate, Titanium Dioxide, and Zinc Oxide |
Active Ingredient(s): | 2.516; .748; 5.542 g/34g; g/34g; g/34g & nbsp; Octinoxate, Titanium Dioxide, and Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52686-224 |
Labeler Name: | SHISEIDO AMERICA INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100201 |
Package NDC: | 52686-224-60 |
Package Description: | 1 TUBE in 1 CARTON (52686-224-60) > 34 g in 1 TUBE |
NDC Code | 52686-224-60 |
Proprietary Name | SHISEIDO SUNCARE ULTIMATE |
Package Description | 1 TUBE in 1 CARTON (52686-224-60) > 34 g in 1 TUBE |
Product NDC | 52686-224 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Titanium Dioxide, and Zinc Oxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | SHISEIDO AMERICA INC. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 2.516; .748; 5.542 |
Strength Unit | g/34g; g/34g; g/34g |
Pharmaceutical Classes |