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Sunscreen
Sunscreen - 35192-008-02 - (SPF 40)
Drug Information of Sunscreen
| Product NDC: | 35192-008 |
| Proprietary Name: | Sunscreen |
| Non Proprietary Name: | SPF 40 |
| Active Ingredient(s): | 8.5; 6.8 g/113.4g; g/113.4g & nbsp; SPF 40 |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunscreen
| Product NDC: | 35192-008 |
| 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 Sunscreen
| Package NDC: | 35192-008-02 |
| Package Description: | 113.4 g in 1 TUBE (35192-008-02) |
NDC Information of Sunscreen
| NDC Code | 35192-008-02 |
| Proprietary Name | Sunscreen |
| Package Description | 113.4 g in 1 TUBE (35192-008-02) |
| Product NDC | 35192-008 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SPF 40 |
| 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 | 8.5; 6.8 |
| Strength Unit | g/113.4g; g/113.4g |
| Pharmaceutical Classes |
