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Face and Body Sunscreen
Face and Body Sunscreen - 67510-0081-5 - (Octinoxate and Titanium dioxide)
Drug Information of Face and Body Sunscreen
| Product NDC: | 67510-0081 |
| Proprietary Name: | Face and Body Sunscreen |
| Non Proprietary Name: | Octinoxate and Titanium dioxide |
| Active Ingredient(s): | 7; 2.8 g/100mL; g/100mL & nbsp; Octinoxate and Titanium dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Face and Body Sunscreen
| Product NDC: | 67510-0081 |
| Labeler Name: | Kareway Product, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130124 |
Package Information of Face and Body Sunscreen
| Package NDC: | 67510-0081-5 |
| Package Description: | 100 mL in 1 TUBE (67510-0081-5) |
NDC Information of Face and Body Sunscreen
| NDC Code | 67510-0081-5 |
| Proprietary Name | Face and Body Sunscreen |
| Package Description | 100 mL in 1 TUBE (67510-0081-5) |
| Product NDC | 67510-0081 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Titanium dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130124 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kareway Product, Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 7; 2.8 |
| Strength Unit | g/100mL; g/100mL |
| Pharmaceutical Classes |
