Product NDC: | 52686-329 |
Proprietary Name: | SHISEIDO FUTURE SOLUTION LX DAYTIME PROTECTIVE |
Non Proprietary Name: | AVOBENZONE, OCTINOXATE, and OCTOCRYLENE |
Active Ingredient(s): | 1255; 3715; 1004 mg/50.2g; mg/50.2g; mg/50.2g & nbsp; AVOBENZONE, OCTINOXATE, and OCTOCRYLENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52686-329 |
Labeler Name: | SHISEIDO AMERICA INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121101 |
Package NDC: | 52686-329-51 |
Package Description: | 1 TUBE in 1 CARTON (52686-329-51) > 3.01 g in 1 TUBE |
NDC Code | 52686-329-51 |
Proprietary Name | SHISEIDO FUTURE SOLUTION LX DAYTIME PROTECTIVE |
Package Description | 1 TUBE in 1 CARTON (52686-329-51) > 3.01 g in 1 TUBE |
Product NDC | 52686-329 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, OCTINOXATE, and OCTOCRYLENE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20121101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | SHISEIDO AMERICA INC. |
Substance Name | AVOBENZONE; OCTINOXATE; OCTOCRYLENE |
Strength Number | 1255; 3715; 1004 |
Strength Unit | mg/50.2g; mg/50.2g; mg/50.2g |
Pharmaceutical Classes |