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Algenist
Algenist - 53407-138-30 - (Octinoxate, Titanium Dioxide, Zinc Oxide)
Drug Information of Algenist
| Product NDC: | 53407-138 |
| Proprietary Name: | Algenist |
| Non Proprietary Name: | Octinoxate, Titanium Dioxide, Zinc Oxide |
| Active Ingredient(s): | 75; 20; 171 mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Titanium Dioxide, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Algenist
| Product NDC: | 53407-138 |
| Labeler Name: | Solazyme, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120801 |
Package Information of Algenist
| Package NDC: | 53407-138-30 |
| Package Description: | 1 CARTON in 1 BOX (53407-138-30) > 1 JAR in 1 CARTON > 30 mL in 1 JAR |
NDC Information of Algenist
| NDC Code | 53407-138-30 |
| Proprietary Name | Algenist |
| Package Description | 1 CARTON in 1 BOX (53407-138-30) > 1 JAR in 1 CARTON > 30 mL in 1 JAR |
| Product NDC | 53407-138 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Titanium Dioxide, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Solazyme, Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 75; 20; 171 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
