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Sun Essential
Sun Essential - 35192-009-05 - (Octinoxate Titanium Dioxide)
Drug Information of Sun Essential
| Product NDC: | 35192-009 |
| Proprietary Name: | Sun Essential |
| Non Proprietary Name: | Octinoxate Titanium Dioxide |
| Active Ingredient(s): | 1.5; 1.2 g/30g; g/30g & nbsp; Octinoxate Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sun Essential
| Product NDC: | 35192-009 |
| Labeler Name: | CA-BOTANA INTERNATIONAL |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120601 |
Package Information of Sun Essential
| Package NDC: | 35192-009-05 |
| Package Description: | 30 g in 1 TUBE (35192-009-05) |
NDC Information of Sun Essential
| NDC Code | 35192-009-05 |
| Proprietary Name | Sun Essential |
| Package Description | 30 g in 1 TUBE (35192-009-05) |
| Product NDC | 35192-009 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CA-BOTANA INTERNATIONAL |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 1.5; 1.2 |
| Strength Unit | g/30g; g/30g |
| Pharmaceutical Classes |
