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Jafra Brightening
Jafra Brightening - 68828-101-01 - (Otinoxate, Zinc Oxide)
Drug Information of Jafra Brightening
| Product NDC: | 68828-101 |
| Proprietary Name: | Jafra Brightening |
| Non Proprietary Name: | Otinoxate, Zinc Oxide |
| Active Ingredient(s): | 2.5; 2 mL/50mL; mL/50mL & nbsp; Otinoxate, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Jafra Brightening
| Product NDC: | 68828-101 |
| Labeler Name: | Jafra Cosmetics International Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120515 |
Package Information of Jafra Brightening
| Package NDC: | 68828-101-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (68828-101-01) > 50 mL in 1 BOTTLE |
NDC Information of Jafra Brightening
| NDC Code | 68828-101-01 |
| Proprietary Name | Jafra Brightening |
| Package Description | 1 BOTTLE in 1 CARTON (68828-101-01) > 50 mL in 1 BOTTLE |
| Product NDC | 68828-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Otinoxate, Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120515 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Jafra Cosmetics International Inc |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 2.5; 2 |
| Strength Unit | mL/50mL; mL/50mL |
| Pharmaceutical Classes |
