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UV ESSENTIEL
UV ESSENTIEL - 68745-1085-1 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of UV ESSENTIEL
| Product NDC: | 68745-1085 |
| Proprietary Name: | UV ESSENTIEL |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | 2.25; .6; 5.13 mL/30mL; mL/30mL; mL/30mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of UV ESSENTIEL
| Product NDC: | 68745-1085 |
| Labeler Name: | CHANEL PARFUMS BEAUTE |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120810 |
Package Information of UV ESSENTIEL
| Package NDC: | 68745-1085-1 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (68745-1085-1) > 30 mL in 1 BOTTLE, PUMP |
NDC Information of UV ESSENTIEL
| NDC Code | 68745-1085-1 |
| Proprietary Name | UV ESSENTIEL |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (68745-1085-1) > 30 mL in 1 BOTTLE, PUMP |
| Product NDC | 68745-1085 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120810 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CHANEL PARFUMS BEAUTE |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 2.25; .6; 5.13 |
| Strength Unit | mL/30mL; mL/30mL; mL/30mL |
| Pharmaceutical Classes |
