| Product NDC: | 52686-335 |
| Proprietary Name: | SHISEIDO SUN PROTECTION EYE |
| Non Proprietary Name: | OCTINOXATE, OCTOCRYLENE, and ZINC OXIDE |
| Active Ingredient(s): | 479; 495; 1749 mg/16.5g; mg/16.5g; mg/16.5g & nbsp; OCTINOXATE, OCTOCRYLENE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52686-335 |
| Labeler Name: | SHISEIDO AMERICA INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121201 |
| Package NDC: | 52686-335-60 |
| Package Description: | 1 TUBE in 1 CARTON (52686-335-60) > 16.5 g in 1 TUBE |
| NDC Code | 52686-335-60 |
| Proprietary Name | SHISEIDO SUN PROTECTION EYE |
| Package Description | 1 TUBE in 1 CARTON (52686-335-60) > 16.5 g in 1 TUBE |
| Product NDC | 52686-335 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTOCRYLENE, and ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SHISEIDO AMERICA INC. |
| Substance Name | OCTINOXATE; OCTOCRYLENE; ZINC OXIDE |
| Strength Number | 479; 495; 1749 |
| Strength Unit | mg/16.5g; mg/16.5g; mg/16.5g |
| Pharmaceutical Classes |