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: | 52686-335-61 |
Package Description: | 1 POUCH in 1 CARTON (52686-335-61) > 1.65 g in 1 POUCH (52686-335-80) |
NDC Code | 52686-335-61 |
Proprietary Name | SHISEIDO SUN PROTECTION EYE |
Package Description | 1 POUCH in 1 CARTON (52686-335-61) > 1.65 g in 1 POUCH (52686-335-80) |
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 |