Product NDC: | 58668-5051 |
Proprietary Name: | Instant Sun Light Bronzing SPF 15 Tint 20 Golden 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: | 58668-5051 |
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: | 58668-5051-1 |
Package Description: | 1 BOTTLE in 1 PACKAGE (58668-5051-1) > 10 g in 1 BOTTLE |
NDC Code | 58668-5051-1 |
Proprietary Name | Instant Sun Light Bronzing SPF 15 Tint 20 Golden Sun |
Package Description | 1 BOTTLE in 1 PACKAGE (58668-5051-1) > 10 g in 1 BOTTLE |
Product NDC | 58668-5051 |
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 |