| Product NDC: | 58668-5931 |
| Proprietary Name: | CLARINS Age-Control Hand SPF 15 |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
| Active Ingredient(s): | 2; 7.5; 5; 5 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58668-5931 |
| Labeler Name: | Laboratoires Clarins S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110324 |
| Package NDC: | 58668-5931-1 |
| Package Description: | 75 mL in 1 BOTTLE (58668-5931-1) |
| NDC Code | 58668-5931-1 |
| Proprietary Name | CLARINS Age-Control Hand SPF 15 |
| Package Description | 75 mL in 1 BOTTLE (58668-5931-1) |
| Product NDC | 58668-5931 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110324 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratoires Clarins S.A. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 2; 7.5; 5; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |