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Sunbar SPF 48
Sunbar SPF 48 - 63550-809-10 - (Ensulizole Homosalate Octinoxate Octocrylene Zinc oxide)
Drug Information of Sunbar SPF 48
| Product NDC: | 63550-809 |
| Proprietary Name: | Sunbar SPF 48 |
| Non Proprietary Name: | Ensulizole Homosalate Octinoxate Octocrylene Zinc oxide |
| Active Ingredient(s): | 30; 100; 75; 70; 80 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Ensulizole Homosalate Octinoxate Octocrylene Zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunbar SPF 48
| Product NDC: | 63550-809 |
| Labeler Name: | Kamins Dermatologics Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100929 |
Package Information of Sunbar SPF 48
| Package NDC: | 63550-809-10 |
| Package Description: | 120 mL in 1 BOX (63550-809-10) |
NDC Information of Sunbar SPF 48
| NDC Code | 63550-809-10 |
| Proprietary Name | Sunbar SPF 48 |
| Package Description | 120 mL in 1 BOX (63550-809-10) |
| Product NDC | 63550-809 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ensulizole Homosalate Octinoxate Octocrylene Zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100929 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kamins Dermatologics Inc. |
| Substance Name | ENSULIZOLE; HOMOSALATE; OCTINOXATE; OCTOCRYLENE; ZINC OXIDE |
| Strength Number | 30; 100; 75; 70; 80 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
