| Product NDC: | 62742-4036 |
| Proprietary Name: | AGELESS Total Rejuvenating Hand |
| Non Proprietary Name: | Octinoxate, Octisalate, Avobenzone, Octocrylene |
| Active Ingredient(s): | 20; 75; 50; 20 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Octisalate, Avobenzone, Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62742-4036 |
| Labeler Name: | Allure Labs, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100101 |
| Package NDC: | 62742-4036-1 |
| Package Description: | 56.7 mL in 1 TUBE (62742-4036-1) |
| NDC Code | 62742-4036-1 |
| Proprietary Name | AGELESS Total Rejuvenating Hand |
| Package Description | 56.7 mL in 1 TUBE (62742-4036-1) |
| Product NDC | 62742-4036 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Avobenzone, Octocrylene |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Allure Labs, Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 20; 75; 50; 20 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |