| Product NDC: | 61016-0003 |
| Proprietary Name: | Anti-Aging Daily Moisturizer Sunscreen Broad-Spectrum SPF 30 |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Active Ingredient(s): | 3; 7.5; 5; 4 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61016-0003 |
| Labeler Name: | Columbia Cosmetics Manufacturing, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120419 |
| Package NDC: | 61016-0003-2 |
| Package Description: | 59 mL in 1 BOTTLE (61016-0003-2) |
| NDC Code | 61016-0003-2 |
| Proprietary Name | Anti-Aging Daily Moisturizer Sunscreen Broad-Spectrum SPF 30 |
| Package Description | 59 mL in 1 BOTTLE (61016-0003-2) |
| Product NDC | 61016-0003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120419 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Columbia Cosmetics Manufacturing, Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 3; 7.5; 5; 4 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |