| Product NDC: | 76209-123 |
| Proprietary Name: | Cellular Laboratories De-Aging Sunscreen Broad Spectrum SPF 50 Plus |
| Non Proprietary Name: | HOMOSALATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
| Active Ingredient(s): | 30; 100; 50; 26 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; HOMOSALATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76209-123 |
| Labeler Name: | Market America |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110503 |
| Package NDC: | 76209-123-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (76209-123-01) > 100 mL in 1 BOTTLE |
| NDC Code | 76209-123-01 |
| Proprietary Name | Cellular Laboratories De-Aging Sunscreen Broad Spectrum SPF 50 Plus |
| Package Description | 1 BOTTLE in 1 CARTON (76209-123-01) > 100 mL in 1 BOTTLE |
| Product NDC | 76209-123 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110503 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Market America |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 30; 100; 50; 26 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |