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CYZONE
CYZONE - 13537-013-15 - (OCTINOXATE and OCTOCRYLENE)
Drug Information of CYZONE
| Product NDC: | 13537-013 |
| Proprietary Name: | CYZONE |
| Non Proprietary Name: | OCTINOXATE and OCTOCRYLENE |
| Active Ingredient(s): | .06; .04 g/g; g/g & nbsp; OCTINOXATE and OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CYZONE
| Product NDC: | 13537-013 |
| Labeler Name: | Ventura Corporation Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110121 |
Package Information of CYZONE
| Package NDC: | 13537-013-15 |
| Package Description: | 1 CONTAINER in 1 CARTON (13537-013-15) > 14 g in 1 CONTAINER (13537-013-14) |
NDC Information of CYZONE
| NDC Code | 13537-013-15 |
| Proprietary Name | CYZONE |
| Package Description | 1 CONTAINER in 1 CARTON (13537-013-15) > 14 g in 1 CONTAINER (13537-013-14) |
| Product NDC | 13537-013 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and OCTOCRYLENE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110121 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ventura Corporation Limited |
| Substance Name | OCTINOXATE; OCTOCRYLENE |
| Strength Number | .06; .04 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
