| 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 |