| Product NDC: | 58668-4031 |
| Proprietary Name: | CLARINS BROAD SPECTRUM SPF 50 Plus - SUNSCREEN FOR FACE WRINKLE CONTROL |
| Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Active Ingredient(s): | 30; 100; 50; 27; 60 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58668-4031 |
| Labeler Name: | Laboratoires Clarins S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130508 |
| Package NDC: | 58668-4031-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (58668-4031-1) > 75 mL in 1 BOTTLE |
| NDC Code | 58668-4031-1 |
| Proprietary Name | CLARINS BROAD SPECTRUM SPF 50 Plus - SUNSCREEN FOR FACE WRINKLE CONTROL |
| Package Description | 1 BOTTLE in 1 CARTON (58668-4031-1) > 75 mL in 1 BOTTLE |
| Product NDC | 58668-4031 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130508 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Laboratoires Clarins S.A. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 100; 50; 27; 60 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |