Product NDC: | 52686-272 |
Proprietary Name: | SHISEIDO URBAN ENVIRONMENT |
Non Proprietary Name: | OCTINOXATE, OCTOCRYLENE, and ZINC OXIDE |
Active Ingredient(s): | 1557; 953; 3971 mg/31.77g; mg/31.77g; mg/31.77g & nbsp; OCTINOXATE, OCTOCRYLENE, and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52686-272 |
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: | 52686-272-10 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (52686-272-10) > 31.77 g in 1 BOTTLE, PLASTIC |
NDC Code | 52686-272-10 |
Proprietary Name | SHISEIDO URBAN ENVIRONMENT |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (52686-272-10) > 31.77 g in 1 BOTTLE, PLASTIC |
Product NDC | 52686-272 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTOCRYLENE, 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; ZINC OXIDE |
Strength Number | 1557; 953; 3971 |
Strength Unit | mg/31.77g; mg/31.77g; mg/31.77g |
Pharmaceutical Classes |