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CYZONE
CYZONE - 13537-449-02 - (Octinoxate and Oxybenzone)
Drug Information of CYZONE
| Product NDC: | 13537-449 |
| Proprietary Name: | CYZONE |
| Non Proprietary Name: | Octinoxate and Oxybenzone |
| Active Ingredient(s): | .075; .045 g/g; g/g & nbsp; Octinoxate and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CYZONE
| Product NDC: | 13537-449 |
| Labeler Name: | Ventura Corporation LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130201 |
Package Information of CYZONE
| Package NDC: | 13537-449-02 |
| Package Description: | 1 BOTTLE in 1 CARTON (13537-449-02) > 50 g in 1 BOTTLE (13537-449-01) |
NDC Information of CYZONE
| NDC Code | 13537-449-02 |
| Proprietary Name | CYZONE |
| Package Description | 1 BOTTLE in 1 CARTON (13537-449-02) > 50 g in 1 BOTTLE (13537-449-01) |
| Product NDC | 13537-449 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ventura Corporation LTD. |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | .075; .045 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
