| Product NDC: | 52686-274 |
| Proprietary Name: | SHISEIDO ULTIMATE SUN PROTECTION PLUS |
| Non Proprietary Name: | OCTINOXATE, OCTOCRYLENE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | 8673; 3516; 1992; 22.62 mg/100mL; mg/100mL; mg/100mL; g/100mL & nbsp; OCTINOXATE, OCTOCRYLENE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52686-274 |
| Labeler Name: | SHISEIDO AMERICA INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121001 |
| Package NDC: | 52686-274-10 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (52686-274-10) > 100 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 52686-274-10 |
| Proprietary Name | SHISEIDO ULTIMATE SUN PROTECTION PLUS |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (52686-274-10) > 100 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 52686-274 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTOCRYLENE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SHISEIDO AMERICA INC. |
| Substance Name | OCTINOXATE; OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 8673; 3516; 1992; 22.62 |
| Strength Unit | mg/100mL; mg/100mL; mg/100mL; g/100mL |
| Pharmaceutical Classes |