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Boscia Daily Defense Sunscreen Broad Spectrum SPF 50 PA
Boscia Daily Defense Sunscreen Broad Spectrum SPF 50 PA - 76151-241-01 - (OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE)
Drug Information of Boscia Daily Defense Sunscreen Broad Spectrum SPF 50 PA
| Product NDC: | 76151-241 |
| Proprietary Name: | Boscia Daily Defense Sunscreen Broad Spectrum SPF 50 PA |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE |
| Active Ingredient(s): | 7.25; 5.742; 4.75 g/100g; g/100g; g/100g & nbsp; OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Boscia Daily Defense Sunscreen Broad Spectrum SPF 50 PA
| Product NDC: | 76151-241 |
| Labeler Name: | Boscia LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121107 |
Package Information of Boscia Daily Defense Sunscreen Broad Spectrum SPF 50 PA
| Package NDC: | 76151-241-01 |
| Package Description: | 50 g in 1 TUBE (76151-241-01) |
NDC Information of Boscia Daily Defense Sunscreen Broad Spectrum SPF 50 PA
| NDC Code | 76151-241-01 |
| Proprietary Name | Boscia Daily Defense Sunscreen Broad Spectrum SPF 50 PA |
| Package Description | 50 g in 1 TUBE (76151-241-01) |
| Product NDC | 76151-241 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121107 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Boscia LLC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 7.25; 5.742; 4.75 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
