| Product NDC: | 76354-016 |
| Proprietary Name: | ELF SPF 45 Sunscreen UVA/UVB Protection |
| Non Proprietary Name: | TITANIUM DIOXIDE |
| Active Ingredient(s): | 23.3; 18.7 g/100g; g/100g & nbsp; TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76354-016 |
| Labeler Name: | J. A. Cosmetics U.S. INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111022 |
| Package NDC: | 76354-016-01 |
| Package Description: | 10 g in 1 BOTTLE (76354-016-01) |
| NDC Code | 76354-016-01 |
| Proprietary Name | ELF SPF 45 Sunscreen UVA/UVB Protection |
| Package Description | 10 g in 1 BOTTLE (76354-016-01) |
| Product NDC | 76354-016 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20111022 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | J. A. Cosmetics U.S. INC |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 23.3; 18.7 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |