Product NDC: | 13537-435 |
Proprietary Name: | CYZONE |
Non Proprietary Name: | Octinoxate, Octocrylene, Oxybenzone, Octisalate, Titanium Dioxide, and Ensulizole |
Active Ingredient(s): | .03; .075; .05; .07; .06; .468 g/g; g/g; g/g; g/g; g/g; g/g & nbsp; Octinoxate, Octocrylene, Oxybenzone, Octisalate, Titanium Dioxide, and Ensulizole |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13537-435 |
Labeler Name: | Ventura Corporation LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120914 |
Package NDC: | 13537-435-01 |
Package Description: | 60 g in 1 TUBE (13537-435-01) |
NDC Code | 13537-435-01 |
Proprietary Name | CYZONE |
Package Description | 60 g in 1 TUBE (13537-435-01) |
Product NDC | 13537-435 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octocrylene, Oxybenzone, Octisalate, Titanium Dioxide, and Ensulizole |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120914 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ventura Corporation LTD. |
Substance Name | ENSULIZOLE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE |
Strength Number | .03; .075; .05; .07; .06; .468 |
Strength Unit | g/g; g/g; g/g; g/g; g/g; g/g |
Pharmaceutical Classes |