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ESIKA
ESIKA - 13537-152-01 - (Octinoxate and Oxybenzone)
Drug Information of ESIKA
| Product NDC: | 13537-152 |
| Proprietary Name: | ESIKA |
| 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 ESIKA
| Product NDC: | 13537-152 |
| Labeler Name: | Ventura Corporation Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120124 |
Package Information of ESIKA
| Package NDC: | 13537-152-01 |
| Package Description: | 60 g in 1 BOTTLE (13537-152-01) |
NDC Information of ESIKA
| NDC Code | 13537-152-01 |
| Proprietary Name | ESIKA |
| Package Description | 60 g in 1 BOTTLE (13537-152-01) |
| Product NDC | 13537-152 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120124 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ventura Corporation Ltd |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | .075; .045 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
