| Product NDC: | 58668-5041 |
| Proprietary Name: | Instant Sun Light Bronzing SPF 15 Tint 10 Morning Sun |
| Non Proprietary Name: | TITANIUM DIOXIDE |
| Active Ingredient(s): | 10.5 g/100g & nbsp; TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58668-5041 |
| Labeler Name: | Laboratoires Clarins S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110114 |
| Package NDC: | 58668-5041-1 |
| Package Description: | 1 BOTTLE in 1 PACKAGE (58668-5041-1) > 10 g in 1 BOTTLE |
| NDC Code | 58668-5041-1 |
| Proprietary Name | Instant Sun Light Bronzing SPF 15 Tint 10 Morning Sun |
| Package Description | 1 BOTTLE in 1 PACKAGE (58668-5041-1) > 10 g in 1 BOTTLE |
| Product NDC | 58668-5041 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20110114 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratoires Clarins S.A. |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | 10.5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |