Product NDC: | 58668-4291 |
Proprietary Name: | Clarins Sunscreen For Face Wrinkle Control SPF 50 Plus |
Non Proprietary Name: | HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
Active Ingredient(s): | 3; 10; 5; 2.7; 6 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58668-4291 |
Labeler Name: | Laboratoires Clarins S.A. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101021 |
Package NDC: | 58668-4291-1 |
Package Description: | 1 BOTTLE in 1 PACKAGE (58668-4291-1) > 75 mL in 1 BOTTLE |
NDC Code | 58668-4291-1 |
Proprietary Name | Clarins Sunscreen For Face Wrinkle Control SPF 50 Plus |
Package Description | 1 BOTTLE in 1 PACKAGE (58668-4291-1) > 75 mL in 1 BOTTLE |
Product NDC | 58668-4291 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20101021 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Laboratoires Clarins S.A. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 3; 10; 5; 2.7; 6 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |